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nsv4382785

  • Variant Calls:75
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:34,852

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1028 SVs from 88 studies. See in: genome view    
Remapped(Score: Perfect):11,064,218-11,099,069Question Mark
Overlapping variant regions from other studies: 1029 SVs from 88 studies. See in: genome view    
Submitted genomic11,216,817-11,251,668Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4382785RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1211,064,21811,099,069
nsv4382785Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1211,216,81711,251,668

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15612302copy number gain1-0678-003SNP arrayGenotyping18
nssv15614901copy number gain1-0706-003SNP arrayGenotyping22
nssv15615283copy number gain1-0766-003SNP arrayGenotyping17
nssv15615870copy number gain1-0789-003SNP arrayGenotyping18
nssv15616276copy number gain1-0144-004SNP arrayGenotyping25
nssv15617537copy number gain1-0828-003SNP arrayGenotyping18
nssv15617860copy number gain1-0854-003SNP arrayGenotyping24
nssv15618938copy number gain1-0896-003SNP arrayGenotyping20
nssv15619805copy number gain1-0909-003SNP arrayGenotyping21
nssv15619829copy number loss1-0910-003SNP arrayGenotyping22
nssv15621235copy number gain1-0989-003SNP arrayGenotyping27
nssv15625642copy number gain1-0345-004SNP arrayGenotyping21
nssv15625843copy number gain1-0389-005SNP arrayGenotyping16
nssv15626330copy number gain1-0413-001SNP arrayGenotyping14
nssv15630699copy number gain1-0602-004SNP arrayGenotyping19
nssv15631250copy number gain1-0616-004SNP arrayGenotyping18
nssv15632215copy number gain10-1090-003SNP arrayGenotyping20
nssv15633869copy number gain10-1149-003SNP arrayGenotyping17
nssv15634469copy number loss11-0043-003SNP arrayGenotyping18
nssv15635711copy number loss11-0054-003SNP arrayGenotyping22
nssv15636253copy number gain14-0036-001SNP arrayGenotyping14
nssv15636809copy number gain13-0161-001SNP arrayGenotyping16
nssv15636856copy number gain13-0161-004SNP arrayGenotyping14
nssv15637328copy number gain13-0094-001SNP arrayGenotyping17
nssv15640476copy number loss14-0325-004SNP arrayGenotyping17
nssv15641146copy number gain14-0384-003SNP arrayGenotyping23
nssv15641658copy number gain14-0243-003SNP arrayGenotyping27
nssv15641684copy number gain14-0246-003SNP arrayGenotyping25
nssv15643294copy number loss14-0364-001SNP arrayGenotyping22
nssv15643736copy number loss2-0122-004SNP arrayGenotyping13
nssv15646517copy number loss2-1268-001SNP arrayGenotyping17
nssv15647884copy number gain2-1305-001SNP arrayGenotyping29
nssv15648135copy number gain2-1352-002SNP arrayGenotyping24
nssv15650067copy number loss2-1292-004SNP arrayGenotyping14
nssv15650404copy number gain2-1478-001SNP arrayGenotyping16
nssv15651225copy number gain2-1369-001SNP arrayGenotyping16
nssv15652001copy number gain2-1508-002SNP arrayGenotyping17
nssv15652322copy number loss2-1486-003SNP arrayGenotyping16
nssv15652471copy number loss2-1519-006SNP arrayGenotyping20
nssv15654640copy number gain3-0178-000SNP arrayGenotyping25
nssv15655856copy number loss2-1743-004SNP arrayGenotyping23
nssv15655943copy number gain2-1750-003SNP arrayGenotyping27
nssv15657759copy number loss4-0048-001SNP arrayGenotyping23
nssv15660042copy number gain5-0004-003SNP arrayGenotyping24
nssv15660269copy number loss3-0719-000SNP arrayGenotyping19
nssv15661423copy number gain5-0083-003SNP arrayGenotyping24
nssv15662468copy number gain5-0049-003SNP arrayGenotyping27
nssv15667812copy number gain7-0129-003SNP arrayGenotyping18
nssv15670484copy number loss7-0175-003SNP arrayGenotyping16
nssv15673793copy number gain9-0013-003SNP arrayGenotyping22
nssv15673857copy number gain9-0024-002SNP arrayGenotyping28
nssv15674684copy number gain185283SNP arrayGenotyping16
nssv15676628copy number gain176714SNP arrayGenotyping18
nssv15677687copy number gain234064SSNP arrayGenotyping27
nssv15677968copy number loss229185SSNP arrayGenotyping28
nssv15679035copy number gain239121SSNP arrayGenotyping20
nssv15684886copy number gainOCD149-MF-1246(189249)SNP arrayGenotyping21
nssv15684995copy number gainOCD157-EB-1282(190114)SNP arrayGenotyping17
nssv15685691copy number lossOCD169-8961253SNP arrayGenotyping21
nssv15686638copy number gainOCD152-SM-1338(188608)SNP arrayGenotyping21
nssv15687467copy number gainOCD161-RS-1449SNP arrayGenotyping24
nssv15687496copy number gainOCD162-896232SNP arrayGenotyping18
nssv15687552copy number gainOCD163-896472SNP arrayGenotyping19
nssv15689332copy number gainOCD100-1570SNP arrayGenotyping23
nssv15690880copy number lossOCD171-BS-363_1771SNP arrayGenotyping15
nssv15694421copy number gainOCD89-0625-2318-2SNP arrayGenotyping28
nssv15695384copy number gain158984SNP arrayGenotyping29
nssv15697228copy number loss155931SNP arrayGenotyping10
nssv15699247copy number gain224900SNP arrayGenotyping15
nssv15699845copy number gain211845SNP arrayGenotyping18
nssv15700368copy number gain205282SNP arrayGenotyping25
nssv15701127copy number loss183323SNP arrayGenotyping26
nssv15701282copy number loss196841SNP arrayGenotyping25
nssv15702378copy number loss153923SNP arrayGenotyping22
nssv15702713copy number gain207953SNP arrayGenotyping16

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15612302RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15614901RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15615283RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15615870RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15616276RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15617537RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15617860RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15618938RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15619805RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15619829RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15621235RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15625642RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15625843RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15626330RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15630699RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15631250RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15632215RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15633869RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15634469RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15635711RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15636253RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15636809RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15636856RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15637328RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15640476RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15641146RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15641658RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15641684RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15643294RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15643736RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15646517RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15647884RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15648135RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15650067RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15650404RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15651225RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15652001RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15652322RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15652471RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15654640RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15655856RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15655943RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15657759RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15660042RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15660269RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15661423RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15662468RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15667812RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15670484RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15673793RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15673857RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15674684RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15676628RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15677687RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15677968RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15679035RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15684886RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15684995RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15685691RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15686638RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15687467RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15687496RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15687552RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15689332RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15690880RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15694421RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15695384RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15697228RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15699247RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15699845RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15700368RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15701127RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15701282RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15702378RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)del
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15702713RemappedPerfectNC_000012.12:g.(?_
11064218)_(1109906
9_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,064,21811,099,069
nssv15612302Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15614901Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15615283Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15615870Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15616276Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15617537Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15617860Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15618938Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15619805Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15619829Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15621235Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15625642Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15625843Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15626330Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15630699Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15631250Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15632215Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15633869Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15634469Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15635711Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15636253Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15636809Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15636856Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15637328Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
nssv15640476Submitted genomicNC_000012.11:g.(?_
11216817)_(1125166
8_?)del
GRCh37 (hg19)NC_000012.11Chr1211,216,81711,251,668
Showing 100 of 150

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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