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nsv4431140

  • Variant Calls:16
  • 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: 233 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):147,118,163-147,118,163Question Mark
Overlapping variant regions from other studies: 193 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):147,685,223-147,685,223Question Mark
Overlapping variant regions from other studies: 192 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):148,124,574-148,124,574Question Mark
Overlapping variant regions from other studies: 196 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):148,636,933-148,636,933Question Mark
Overlapping variant regions from other studies: 116 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):84,057,622-84,057,622Question Mark
Overlapping variant regions from other studies: 110 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):84,128,458-84,128,458Question Mark
Overlapping variant regions from other studies: 111 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):85,066,858-85,066,858Question Mark
Overlapping variant regions from other studies: 287 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):89,307,555-89,307,555Question Mark
Overlapping variant regions from other studies: 287 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):89,307,567-89,307,567Question Mark
Overlapping variant regions from other studies: 291 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):89,357,297-89,357,297Question Mark
Overlapping variant regions from other studies: 109 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):91,634,022-91,634,022Question Mark
Overlapping variant regions from other studies: 98 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):93,283,639-93,283,639Question Mark
Overlapping variant regions from other studies: 107 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):93,749,874-93,749,874Question Mark
Overlapping variant regions from other studies: 106 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):93,753,781-93,753,781Question Mark
Overlapping variant regions from other studies: 106 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):93,754,054-93,754,054Question Mark
Overlapping variant regions from other studies: 113 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):94,354,065-94,354,065Question Mark
Overlapping variant regions from other studies: 172 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):101,700,451-101,700,451Question Mark
Overlapping variant regions from other studies: 172 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):101,700,456-101,700,456Question Mark
Overlapping variant regions from other studies: 215 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):102,284,825-102,284,825Question Mark
Overlapping variant regions from other studies: 178 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):103,064,766-103,064,766Question Mark
Overlapping variant regions from other studies: 179 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):103,079,211-103,079,211Question Mark
Overlapping variant regions from other studies: 179 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):103,079,212-103,079,212Question Mark
Overlapping variant regions from other studies: 201 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):104,066,766-104,066,766Question Mark
Overlapping variant regions from other studies: 256 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):114,153,930-114,153,930Question Mark
Overlapping variant regions from other studies: 260 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):114,309,797-114,309,797Question Mark
Overlapping variant regions from other studies: 160 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):96,021,300-96,021,300Question Mark
Overlapping variant regions from other studies: 129 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):23,172,376-23,172,376Question Mark
Overlapping variant regions from other studies: 129 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):23,173,253-23,173,253Question Mark
Overlapping variant regions from other studies: 135 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):24,197,740-24,197,740Question Mark
Overlapping variant regions from other studies: 156 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):25,076,624-25,076,624Question 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):26,063,904-26,063,904Question Mark
Overlapping variant regions from other studies: 233 SVs from 24 studies. See in: genome view    
Submitted genomic146,815,255-146,815,255Question Mark
Overlapping variant regions from other studies: 193 SVs from 21 studies. See in: genome view    
Submitted genomic147,382,315-147,382,315Question Mark
Overlapping variant regions from other studies: 192 SVs from 22 studies. See in: genome view    
Submitted genomic147,821,666-147,821,666Question Mark
Overlapping variant regions from other studies: 196 SVs from 24 studies. See in: genome view    
Submitted genomic148,334,025-148,334,025Question Mark
Overlapping variant regions from other studies: 116 SVs from 29 studies. See in: genome view    
Submitted genomic83,686,938-83,686,938Question Mark
Overlapping variant regions from other studies: 110 SVs from 29 studies. See in: genome view    
Submitted genomic83,757,774-83,757,774Question Mark
Overlapping variant regions from other studies: 111 SVs from 29 studies. See in: genome view    
Submitted genomic84,696,174-84,696,174Question Mark
Overlapping variant regions from other studies: 287 SVs from 46 studies. See in: genome view    
Submitted genomic88,936,869-88,936,869Question Mark
Overlapping variant regions from other studies: 287 SVs from 46 studies. See in: genome view    
Submitted genomic88,936,881-88,936,881Question Mark
Overlapping variant regions from other studies: 291 SVs from 46 studies. See in: genome view    
Submitted genomic88,986,611-88,986,611Question Mark
Overlapping variant regions from other studies: 109 SVs from 29 studies. See in: genome view    
Submitted genomic91,263,337-91,263,337Question Mark
Overlapping variant regions from other studies: 98 SVs from 27 studies. See in: genome view    
Submitted genomic92,912,951-92,912,951Question Mark
Overlapping variant regions from other studies: 107 SVs from 29 studies. See in: genome view    
Submitted genomic93,379,186-93,379,186Question Mark
Overlapping variant regions from other studies: 106 SVs from 28 studies. See in: genome view    
Submitted genomic93,383,093-93,383,093Question Mark
Overlapping variant regions from other studies: 106 SVs from 28 studies. See in: genome view    
Submitted genomic93,383,366-93,383,366Question Mark
Overlapping variant regions from other studies: 113 SVs from 29 studies. See in: genome view    
Submitted genomic93,983,377-93,983,377Question Mark
Overlapping variant regions from other studies: 172 SVs from 17 studies. See in: genome view    
Submitted genomic102,712,679-102,712,679Question Mark
Overlapping variant regions from other studies: 172 SVs from 17 studies. See in: genome view    
Submitted genomic102,712,684-102,712,684Question Mark
Overlapping variant regions from other studies: 215 SVs from 26 studies. See in: genome view    
Submitted genomic103,297,053-103,297,053Question Mark
Overlapping variant regions from other studies: 178 SVs from 17 studies. See in: genome view    
Submitted genomic104,076,994-104,076,994Question Mark
Overlapping variant regions from other studies: 179 SVs from 17 studies. See in: genome view    
Submitted genomic104,091,439-104,091,439Question Mark
Overlapping variant regions from other studies: 179 SVs from 17 studies. See in: genome view    
Submitted genomic104,091,440-104,091,440Question Mark
Overlapping variant regions from other studies: 201 SVs from 26 studies. See in: genome view    
Submitted genomic105,078,994-105,078,994Question Mark
Overlapping variant regions from other studies: 256 SVs from 35 studies. See in: genome view    
Submitted genomic115,166,159-115,166,159Question Mark
Overlapping variant regions from other studies: 260 SVs from 36 studies. See in: genome view    
Submitted genomic115,322,026-115,322,026Question Mark
Overlapping variant regions from other studies: 160 SVs from 18 studies. See in: genome view    
Submitted genomic97,033,528-97,033,528Question Mark
Overlapping variant regions from other studies: 129 SVs from 33 studies. See in: genome view    
Submitted genomic23,193,922-23,193,922Question Mark
Overlapping variant regions from other studies: 129 SVs from 33 studies. See in: genome view    
Submitted genomic23,194,799-23,194,799Question Mark
Overlapping variant regions from other studies: 135 SVs from 29 studies. See in: genome view    
Submitted genomic24,219,286-24,219,286Question Mark
Overlapping variant regions from other studies: 156 SVs from 37 studies. See in: genome view    
Submitted genomic25,098,170-25,098,170Question 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 genomic26,085,451-26,085,451Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7147,118,163147,118,163+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7147,685,223147,685,223+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7148,124,574148,124,574+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7148,636,933148,636,933+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr784,057,62284,057,622-
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr784,128,45884,128,458-
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr785,066,85885,066,858-
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr789,307,55589,307,555-
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr789,307,56789,307,567+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr789,357,29789,357,297+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr791,634,02291,634,022+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr793,283,63993,283,639+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr793,749,87493,749,874-
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr793,753,78193,753,781-
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr793,754,05493,754,054+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr794,354,06594,354,065+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8101,700,451101,700,451+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8101,700,456101,700,456+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8102,284,825102,284,825+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8103,064,766103,064,766-
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8103,079,211103,079,211-
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8103,079,212103,079,212-
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8104,066,766104,066,766-
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8114,153,930114,153,930+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8114,309,797114,309,797+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr896,021,30096,021,300+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1123,172,37623,172,376-
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1123,173,25323,173,253+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1124,197,74024,197,740+
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1125,076,62425,076,624-
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1125,533,36825,533,368-
nsv4431140RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1126,063,90426,063,904-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7146,815,255146,815,255+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7147,382,315147,382,315+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7147,821,666147,821,666+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7148,334,025148,334,025+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr783,686,93883,686,938-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr783,757,77483,757,774-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr784,696,17484,696,174-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr788,936,86988,936,869-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr788,936,88188,936,881+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr788,986,61188,986,611+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr791,263,33791,263,337+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr792,912,95192,912,951+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr793,379,18693,379,186-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr793,383,09393,383,093-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr793,383,36693,383,366+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr793,983,37793,983,377+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8102,712,679102,712,679+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8102,712,684102,712,684+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8103,297,053103,297,053+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8104,076,994104,076,994-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8104,091,439104,091,439-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8104,091,440104,091,440-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8105,078,994105,078,994-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8115,166,159115,166,159+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8115,322,026115,322,026+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr897,033,52897,033,528+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1123,193,92223,193,922-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1123,194,79923,194,799+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1124,219,28624,219,286+
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1125,098,17025,098,170-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1125,554,91425,554,914-
nsv4431140Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1126,085,45126,085,451-

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15745533interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745532intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745530intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745529intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745539intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745540intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745538interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745531intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745541interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745528interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745536intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745537intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745542intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745543interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745535interchromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41
nssv15745534intrachromosomal translocationD15358SequencingPaired-end mapping, Sequence alignment41

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv15745533RemappedPerfectGRCh38.p12First PassNC_000007.14Chr784,057,62284,057,622-
nssv15745532RemappedPerfectGRCh38.p12First PassNC_000007.14Chr784,128,45884,128,458-
nssv15745530RemappedPerfectGRCh38.p12First PassNC_000007.14Chr785,066,85885,066,858-
nssv15745529RemappedPerfectGRCh38.p12First PassNC_000007.14Chr789,307,55589,307,555-
nssv15745539RemappedPerfectGRCh38.p12First PassNC_000007.14Chr789,307,56789,307,567+
nssv15745540RemappedPerfectGRCh38.p12First PassNC_000007.14Chr789,357,29789,357,297+
nssv15745538RemappedPerfectGRCh38.p12First PassNC_000007.14Chr791,634,02291,634,022+
nssv15745539RemappedPerfectGRCh38.p12First PassNC_000007.14Chr793,283,63993,283,639+
nssv15745532RemappedPerfectGRCh38.p12First PassNC_000007.14Chr793,749,87493,749,874-
nssv15745531RemappedPerfectGRCh38.p12First PassNC_000007.14Chr793,753,78193,753,781-
nssv15745530RemappedPerfectGRCh38.p12First PassNC_000007.14Chr793,754,05493,754,054+
nssv15745531RemappedPerfectGRCh38.p12First PassNC_000007.14Chr794,354,06594,354,065+
nssv15745540RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7147,118,163147,118,163+
nssv15745541RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7147,685,223147,685,223+
nssv15745528RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7148,124,574148,124,574+
nssv15745529RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7148,636,933148,636,933+
nssv15745536RemappedPerfectGRCh38.p12First PassNC_000008.11Chr896,021,30096,021,300+
nssv15745541RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8101,700,451101,700,451+
nssv15745537RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8101,700,456101,700,456+
nssv15745542RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8102,284,825102,284,825+
nssv15745538RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8103,064,766103,064,766-
nssv15745543RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8103,079,211103,079,211-
nssv15745537RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8103,079,212103,079,212-
nssv15745542RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8104,066,766104,066,766-
nssv15745535RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8114,153,930114,153,930+
nssv15745536RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8114,309,797114,309,797+
nssv15745543RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1123,172,37623,172,376-
nssv15745533RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1123,173,25323,173,253+
nssv15745534RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1124,197,74024,197,740+
nssv15745535RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1125,076,62425,076,624-
nssv15745534RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1125,533,36825,533,368-
nssv15745528RemappedPerfectGRCh38.p12First PassNC_000011.10Chr1126,063,90426,063,904-
nssv15745533Submitted genomicGRCh37 (hg19)NC_000007.13Chr783,686,93883,686,938-
nssv15745532Submitted genomicGRCh37 (hg19)NC_000007.13Chr783,757,77483,757,774-
nssv15745530Submitted genomicGRCh37 (hg19)NC_000007.13Chr784,696,17484,696,174-
nssv15745529Submitted genomicGRCh37 (hg19)NC_000007.13Chr788,936,86988,936,869-
nssv15745539Submitted genomicGRCh37 (hg19)NC_000007.13Chr788,936,88188,936,881+
nssv15745540Submitted genomicGRCh37 (hg19)NC_000007.13Chr788,986,61188,986,611+
nssv15745538Submitted genomicGRCh37 (hg19)NC_000007.13Chr791,263,33791,263,337+
nssv15745539Submitted genomicGRCh37 (hg19)NC_000007.13Chr792,912,95192,912,951+
nssv15745532Submitted genomicGRCh37 (hg19)NC_000007.13Chr793,379,18693,379,186-
nssv15745531Submitted genomicGRCh37 (hg19)NC_000007.13Chr793,383,09393,383,093-
nssv15745530Submitted genomicGRCh37 (hg19)NC_000007.13Chr793,383,36693,383,366+
nssv15745531Submitted genomicGRCh37 (hg19)NC_000007.13Chr793,983,37793,983,377+
nssv15745540Submitted genomicGRCh37 (hg19)NC_000007.13Chr7146,815,255146,815,255+
nssv15745541Submitted genomicGRCh37 (hg19)NC_000007.13Chr7147,382,315147,382,315+
nssv15745528Submitted genomicGRCh37 (hg19)NC_000007.13Chr7147,821,666147,821,666+
nssv15745529Submitted genomicGRCh37 (hg19)NC_000007.13Chr7148,334,025148,334,025+
nssv15745536Submitted genomicGRCh37 (hg19)NC_000008.10Chr897,033,52897,033,528+
nssv15745541Submitted genomicGRCh37 (hg19)NC_000008.10Chr8102,712,679102,712,679+
nssv15745537Submitted genomicGRCh37 (hg19)NC_000008.10Chr8102,712,684102,712,684+
nssv15745542Submitted genomicGRCh37 (hg19)NC_000008.10Chr8103,297,053103,297,053+
nssv15745538Submitted genomicGRCh37 (hg19)NC_000008.10Chr8104,076,994104,076,994-
nssv15745543Submitted genomicGRCh37 (hg19)NC_000008.10Chr8104,091,439104,091,439-
nssv15745537Submitted genomicGRCh37 (hg19)NC_000008.10Chr8104,091,440104,091,440-
nssv15745542Submitted genomicGRCh37 (hg19)NC_000008.10Chr8105,078,994105,078,994-
nssv15745535Submitted genomicGRCh37 (hg19)NC_000008.10Chr8115,166,159115,166,159+
nssv15745536Submitted genomicGRCh37 (hg19)NC_000008.10Chr8115,322,026115,322,026+
nssv15745543Submitted genomicGRCh37 (hg19)NC_000011.9Chr1123,193,92223,193,922-
nssv15745533Submitted genomicGRCh37 (hg19)NC_000011.9Chr1123,194,79923,194,799+
nssv15745534Submitted genomicGRCh37 (hg19)NC_000011.9Chr1124,219,28624,219,286+
nssv15745535Submitted genomicGRCh37 (hg19)NC_000011.9Chr1125,098,17025,098,170-
nssv15745534Submitted genomicGRCh37 (hg19)NC_000011.9Chr1125,554,91425,554,914-
nssv15745528Submitted genomicGRCh37 (hg19)NC_000011.9Chr1126,085,45126,085,451-

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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