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nsv4431139

  • Variant Calls:17
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):106,878,558-106,878,558Question Mark
Overlapping variant regions from other studies: 118 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):108,361,601-108,361,601Question Mark
Overlapping variant regions from other studies: 118 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):108,361,610-108,361,610Question Mark
Overlapping variant regions from other studies: 119 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):108,745,152-108,745,152Question Mark
Overlapping variant regions from other studies: 119 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):108,745,152-108,745,152Question Mark
Overlapping variant regions from other studies: 151 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):119,857,678-119,857,678Question Mark
Overlapping variant regions from other studies: 151 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):119,857,755-119,857,755Question Mark
Overlapping variant regions from other studies: 125 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):120,068,423-120,068,423Question Mark
Overlapping variant regions from other studies: 125 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):120,068,430-120,068,430Question Mark
Overlapping variant regions from other studies: 130 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):120,130,277-120,130,277Question Mark
Overlapping variant regions from other studies: 159 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):143,373,774-143,373,774Question Mark
Overlapping variant regions from other studies: 416 SVs from 67 studies. See in: genome view    
Remapped(Score: Perfect):143,845,093-143,845,093Question Mark
Overlapping variant regions from other studies: 169 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):145,141,406-145,141,406Question Mark
Overlapping variant regions from other studies: 233 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):147,118,153-147,118,153Question Mark
Overlapping variant regions from other studies: 193 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):147,685,221-147,685,221Question Mark
Overlapping variant regions from other studies: 203 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):147,809,475-147,809,475Question Mark
Overlapping variant regions from other studies: 203 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):147,809,480-147,809,480Question Mark
Overlapping variant regions from other studies: 192 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):148,124,576-148,124,576Question Mark
Overlapping variant regions from other studies: 110 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):84,128,457-84,128,457Question Mark
Overlapping variant regions from other studies: 111 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):85,066,842-85,066,842Question Mark
Overlapping variant regions from other studies: 105 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):91,455,185-91,455,185Question Mark
Overlapping variant regions from other studies: 109 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):91,634,019-91,634,019Question Mark
Overlapping variant regions from other studies: 98 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):93,283,771-93,283,771Question Mark
Overlapping variant regions from other studies: 107 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):93,749,873-93,749,873Question Mark
Overlapping variant regions from other studies: 215 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):102,284,824-102,284,824Question Mark
Overlapping variant regions from other studies: 178 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):103,064,765-103,064,765Question Mark
Overlapping variant regions from other studies: 201 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):104,066,758-104,066,758Question Mark
Overlapping variant regions from other studies: 206 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):113,632,610-113,632,610Question Mark
Overlapping variant regions from other studies: 160 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):96,021,303-96,021,303Question Mark
Overlapping variant regions from other studies: 135 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):24,197,754-24,197,754Question Mark
Overlapping variant regions from other studies: 156 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):25,076,602-25,076,602Question Mark
Overlapping variant regions from other studies: 126 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):25,533,368-25,533,368Question Mark
Overlapping variant regions from other studies: 115 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):26,063,910-26,063,910Question Mark
Overlapping variant regions from other studies: 243 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):62,627,748-62,627,748Question Mark
Overlapping variant regions from other studies: 108 SVs from 22 studies. See in: genome view    
Submitted genomic106,519,003-106,519,003Question Mark
Overlapping variant regions from other studies: 118 SVs from 30 studies. See in: genome view    
Submitted genomic108,002,045-108,002,045Question Mark
Overlapping variant regions from other studies: 118 SVs from 30 studies. See in: genome view    
Submitted genomic108,002,054-108,002,054Question Mark
Overlapping variant regions from other studies: 119 SVs from 28 studies. See in: genome view    
Submitted genomic108,385,596-108,385,596Question Mark
Overlapping variant regions from other studies: 119 SVs from 28 studies. See in: genome view    
Submitted genomic108,385,596-108,385,596Question Mark
Overlapping variant regions from other studies: 151 SVs from 33 studies. See in: genome view    
Submitted genomic119,497,732-119,497,732Question Mark
Overlapping variant regions from other studies: 151 SVs from 33 studies. See in: genome view    
Submitted genomic119,497,809-119,497,809Question Mark
Overlapping variant regions from other studies: 125 SVs from 29 studies. See in: genome view    
Submitted genomic119,708,477-119,708,477Question Mark
Overlapping variant regions from other studies: 125 SVs from 29 studies. See in: genome view    
Submitted genomic119,708,484-119,708,484Question Mark
Overlapping variant regions from other studies: 130 SVs from 31 studies. See in: genome view    
Submitted genomic119,770,331-119,770,331Question Mark
Overlapping variant regions from other studies: 159 SVs from 24 studies. See in: genome view    
Submitted genomic143,070,867-143,070,867Question Mark
Overlapping variant regions from other studies: 416 SVs from 67 studies. See in: genome view    
Submitted genomic143,542,186-143,542,186Question Mark
Overlapping variant regions from other studies: 169 SVs from 26 studies. See in: genome view    
Submitted genomic144,838,499-144,838,499Question Mark
Overlapping variant regions from other studies: 233 SVs from 24 studies. See in: genome view    
Submitted genomic146,815,245-146,815,245Question Mark
Overlapping variant regions from other studies: 193 SVs from 21 studies. See in: genome view    
Submitted genomic147,382,313-147,382,313Question Mark
Overlapping variant regions from other studies: 203 SVs from 26 studies. See in: genome view    
Submitted genomic147,506,567-147,506,567Question Mark
Overlapping variant regions from other studies: 203 SVs from 26 studies. See in: genome view    
Submitted genomic147,506,572-147,506,572Question Mark
Overlapping variant regions from other studies: 192 SVs from 22 studies. See in: genome view    
Submitted genomic147,821,668-147,821,668Question Mark
Overlapping variant regions from other studies: 110 SVs from 29 studies. See in: genome view    
Submitted genomic83,757,773-83,757,773Question Mark
Overlapping variant regions from other studies: 111 SVs from 29 studies. See in: genome view    
Submitted genomic84,696,158-84,696,158Question Mark
Overlapping variant regions from other studies: 105 SVs from 26 studies. See in: genome view    
Submitted genomic91,084,500-91,084,500Question Mark
Overlapping variant regions from other studies: 109 SVs from 29 studies. See in: genome view    
Submitted genomic91,263,334-91,263,334Question Mark
Overlapping variant regions from other studies: 98 SVs from 27 studies. See in: genome view    
Submitted genomic92,913,083-92,913,083Question Mark
Overlapping variant regions from other studies: 107 SVs from 29 studies. See in: genome view    
Submitted genomic93,379,185-93,379,185Question Mark
Overlapping variant regions from other studies: 215 SVs from 26 studies. See in: genome view    
Submitted genomic103,297,052-103,297,052Question Mark
Overlapping variant regions from other studies: 178 SVs from 17 studies. See in: genome view    
Submitted genomic104,076,993-104,076,993Question Mark
Overlapping variant regions from other studies: 201 SVs from 26 studies. See in: genome view    
Submitted genomic105,078,986-105,078,986Question Mark
Overlapping variant regions from other studies: 206 SVs from 21 studies. See in: genome view    
Submitted genomic114,644,839-114,644,839Question Mark
Overlapping variant regions from other studies: 160 SVs from 18 studies. See in: genome view    
Submitted genomic97,033,531-97,033,531Question Mark
Overlapping variant regions from other studies: 135 SVs from 29 studies. See in: genome view    
Submitted genomic24,219,300-24,219,300Question Mark
Overlapping variant regions from other studies: 156 SVs from 37 studies. See in: genome view    
Submitted genomic25,098,148-25,098,148Question Mark
Overlapping variant regions from other studies: 126 SVs from 33 studies. See in: genome view    
Submitted genomic25,554,914-25,554,914Question Mark
Overlapping variant regions from other studies: 115 SVs from 30 studies. See in: genome view    
Submitted genomic26,085,457-26,085,457Question Mark
Overlapping variant regions from other studies: 243 SVs from 25 studies. See in: genome view    
Submitted genomic63,201,881-63,201,881Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7106,878,558106,878,558+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7108,361,601108,361,601-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7108,361,610108,361,610+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7108,745,152108,745,152+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7108,745,152108,745,152-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7119,857,678119,857,678+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7119,857,755119,857,755+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7120,068,423120,068,423+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7120,068,430120,068,430+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7120,130,277120,130,277+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7143,373,774143,373,774-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7143,845,093143,845,093-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7145,141,406145,141,406-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7147,118,153147,118,153-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7147,685,221147,685,221+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7147,809,475147,809,475+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7147,809,480147,809,480+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7148,124,576148,124,576+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr784,128,45784,128,457-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr785,066,84285,066,842-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr791,455,18591,455,185+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr791,634,01991,634,019+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr793,283,77193,283,771+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr793,749,87393,749,873+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8102,284,824102,284,824+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8103,064,765103,064,765+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8104,066,758104,066,758-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8113,632,610113,632,610-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr896,021,30396,021,303+
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1124,197,75424,197,754-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1125,076,60225,076,602-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1125,533,36825,533,368-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1126,063,91026,063,910-
nsv4431139RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1362,627,74862,627,748+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7106,519,003106,519,003+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7108,002,045108,002,045-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7108,002,054108,002,054+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7108,385,596108,385,596+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7108,385,596108,385,596-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7119,497,732119,497,732+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7119,497,809119,497,809+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7119,708,477119,708,477+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7119,708,484119,708,484+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7119,770,331119,770,331+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7143,070,867143,070,867-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7143,542,186143,542,186-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7144,838,499144,838,499-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7146,815,245146,815,245-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7147,382,313147,382,313+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7147,506,567147,506,567+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7147,506,572147,506,572+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7147,821,668147,821,668+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr783,757,77383,757,773-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr784,696,15884,696,158-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr791,084,50091,084,500+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr791,263,33491,263,334+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr792,913,08392,913,083+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr793,379,18593,379,185+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8103,297,052103,297,052+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8104,076,993104,076,993+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8105,078,986105,078,986-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8114,644,839114,644,839-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr897,033,53197,033,531+
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1124,219,30024,219,300-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1125,098,14825,098,148-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1125,554,91425,554,914-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1126,085,45726,085,457-
nsv4431139Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1363,201,88163,201,881+

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15745559intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745560interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745558intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745557intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745524intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745523intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745525intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745522intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745526intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745527interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745553interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745556intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745562interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745561interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745555interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745545intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745554intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv15745559RemappedPerfectGRCh38.p12First PassNC_000007.14Chr784,128,45784,128,457-
nssv15745560RemappedPerfectGRCh38.p12First PassNC_000007.14Chr785,066,84285,066,842-
nssv15745558RemappedPerfectGRCh38.p12First PassNC_000007.14Chr791,455,18591,455,185+
nssv15745557RemappedPerfectGRCh38.p12First PassNC_000007.14Chr791,634,01991,634,019+
nssv15745559RemappedPerfectGRCh38.p12First PassNC_000007.14Chr793,283,77193,283,771+
nssv15745558RemappedPerfectGRCh38.p12First PassNC_000007.14Chr793,749,87393,749,873+
nssv15745524RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7106,878,558106,878,558+
nssv15745523RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7108,361,601108,361,601-
nssv15745525RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7108,361,610108,361,610+
nssv15745522RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7108,745,152108,745,152-
nssv15745523RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7108,745,152108,745,152+
nssv15745526RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7119,857,678119,857,678+
nssv15745524RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7119,857,755119,857,755+
nssv15745527RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7120,068,423120,068,423+
nssv15745525RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7120,068,430120,068,430+
nssv15745526RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7120,130,277120,130,277+
nssv15745522RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7143,373,774143,373,774-
nssv15745553RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7143,845,093143,845,093-
nssv15745556RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7145,141,406145,141,406-
nssv15745557RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7147,118,153147,118,153-
nssv15745562RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7147,685,221147,685,221+
nssv15745556RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7147,809,475147,809,475+
nssv15745561RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7147,809,480147,809,480+
nssv15745555RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7148,124,576148,124,576+
nssv15745545RemappedPerfectGRCh38.p12First PassNC_000008.11Chr896,021,30396,021,303+
nssv15745561RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8102,284,824102,284,824+
nssv15745560RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8103,064,765103,064,765+
nssv15745562RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8104,066,758104,066,758-
nssv15745545RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8113,632,610113,632,610-
nssv15745553RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1124,197,75424,197,754-
nssv15745554RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1125,076,60225,076,602-
nssv15745554RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1125,533,36825,533,368-
nssv15745555RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1126,063,91026,063,910-
nssv15745527RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1362,627,74862,627,748+
nssv15745559Submitted genomicGRCh37 (hg19)NC_000007.13Chr783,757,77383,757,773-
nssv15745560Submitted genomicGRCh37 (hg19)NC_000007.13Chr784,696,15884,696,158-
nssv15745558Submitted genomicGRCh37 (hg19)NC_000007.13Chr791,084,50091,084,500+
nssv15745557Submitted genomicGRCh37 (hg19)NC_000007.13Chr791,263,33491,263,334+
nssv15745559Submitted genomicGRCh37 (hg19)NC_000007.13Chr792,913,08392,913,083+
nssv15745558Submitted genomicGRCh37 (hg19)NC_000007.13Chr793,379,18593,379,185+
nssv15745524Submitted genomicGRCh37 (hg19)NC_000007.13Chr7106,519,003106,519,003+
nssv15745523Submitted genomicGRCh37 (hg19)NC_000007.13Chr7108,002,045108,002,045-
nssv15745525Submitted genomicGRCh37 (hg19)NC_000007.13Chr7108,002,054108,002,054+
nssv15745522Submitted genomicGRCh37 (hg19)NC_000007.13Chr7108,385,596108,385,596-
nssv15745523Submitted genomicGRCh37 (hg19)NC_000007.13Chr7108,385,596108,385,596+
nssv15745526Submitted genomicGRCh37 (hg19)NC_000007.13Chr7119,497,732119,497,732+
nssv15745524Submitted genomicGRCh37 (hg19)NC_000007.13Chr7119,497,809119,497,809+
nssv15745527Submitted genomicGRCh37 (hg19)NC_000007.13Chr7119,708,477119,708,477+
nssv15745525Submitted genomicGRCh37 (hg19)NC_000007.13Chr7119,708,484119,708,484+
nssv15745526Submitted genomicGRCh37 (hg19)NC_000007.13Chr7119,770,331119,770,331+
nssv15745522Submitted genomicGRCh37 (hg19)NC_000007.13Chr7143,070,867143,070,867-
nssv15745553Submitted genomicGRCh37 (hg19)NC_000007.13Chr7143,542,186143,542,186-
nssv15745556Submitted genomicGRCh37 (hg19)NC_000007.13Chr7144,838,499144,838,499-
nssv15745557Submitted genomicGRCh37 (hg19)NC_000007.13Chr7146,815,245146,815,245-
nssv15745562Submitted genomicGRCh37 (hg19)NC_000007.13Chr7147,382,313147,382,313+
nssv15745556Submitted genomicGRCh37 (hg19)NC_000007.13Chr7147,506,567147,506,567+
nssv15745561Submitted genomicGRCh37 (hg19)NC_000007.13Chr7147,506,572147,506,572+
nssv15745555Submitted genomicGRCh37 (hg19)NC_000007.13Chr7147,821,668147,821,668+
nssv15745545Submitted genomicGRCh37 (hg19)NC_000008.10Chr897,033,53197,033,531+
nssv15745561Submitted genomicGRCh37 (hg19)NC_000008.10Chr8103,297,052103,297,052+
nssv15745560Submitted genomicGRCh37 (hg19)NC_000008.10Chr8104,076,993104,076,993+
nssv15745562Submitted genomicGRCh37 (hg19)NC_000008.10Chr8105,078,986105,078,986-
nssv15745545Submitted genomicGRCh37 (hg19)NC_000008.10Chr8114,644,839114,644,839-
nssv15745553Submitted genomicGRCh37 (hg19)NC_000011.9Chr1124,219,30024,219,300-
nssv15745554Submitted genomicGRCh37 (hg19)NC_000011.9Chr1125,098,14825,098,148-
nssv15745554Submitted genomicGRCh37 (hg19)NC_000011.9Chr1125,554,91425,554,914-
nssv15745555Submitted genomicGRCh37 (hg19)NC_000011.9Chr1126,085,45726,085,457-
nssv15745527Submitted genomicGRCh37 (hg19)NC_000013.10Chr1363,201,88163,201,881+

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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