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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5702414mobile element insertion2nstd211human GRCh38 chr9: 92,644,795-92,644,795 , GRCh37.p13 chr9: 95,407,077-95,407,077 IPPK
    nsv5562344sequence alteration1nstd206human GRCh38 chr9: 92,266,854-92,881,037 , GRCh37.p13 chr9: 95,029,136-95,643,319 ECM2, BICD2, 21 more genes
    nsv5482037copy number variation1nstd206human GRCh38 chr9: 92,670,549-92,670,612 , GRCh37.p13 chr9: 95,432,831-95,432,894 IPPK, LOC107987095
    nsv5481866copy number variation1nstd206human GRCh38 chr9: 92,413,442-92,647,793 , GRCh37.p13 chr9: 95,175,724-95,410,075 ECM2, OMD, 5 more genes
    nsv5413653mobile element insertion1nstd206human GRCh38 chr9: 92,644,795-92,644,846 , GRCh37.p13 chr9: 95,407,077-95,407,128 IPPK
    nsv5131556mobile element insertion1nstd203human GRCh38 chr9: 92,622,397-92,622,410 , GRCh37.p13 chr9: 95,384,679-95,384,692 IPPK
    nsv4887530inversion1nstd200human GRCh37 chr9: 90,662,371-96,951,001 , GRCh38.p12 chr9: 88,047,456-94,188,719 , MTATP6P29, 125 more genes
    nsv4729606copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,175,351-95,375,366 , GRCh38.p12 chr9: 92,413,069-92,613,084 IPPK, ECM2, 4 more genes
    nsv4675239copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,079,793-95,503,060 , GRCh38.p12 chr9: 92,317,511-92,740,778 CENPP, LOC100420779, 11 more genes
    nsv4487512mobile element insertion1nstd166human GRCh37.p13 chr9: 95,407,059-95,407,059 , GRCh38.p12 chr9: 92,644,777-92,644,777 IPPK
    nsv4480342mobile element insertion1nstd166human GRCh37.p13 chr9: 95,395,087-95,395,087 , GRCh38.p12 chr9: 92,632,805-92,632,805 IPPK
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456395copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,123,353-95,453,320 , GRCh38.p12 chr9: 92,361,071-92,691,038 OGN, MIR4670, 8 more genes
    nsv4456112copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,258,118-95,888,821 , GRCh38.p12 chr9: 92,495,836-93,126,539 IPPK, FGD3, 21 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4349215copy number variation1nstd102humanPathogenic GRCh37 chr9: 79,520,825-97,201,274 , GRCh38.p12 chr9: 76,905,909-94,438,992 SPATA31C1, LINC02893, 280 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv3926557copy number variation1nstd167human GRCh37 chr9: 95,386,998-95,387,029 , GRCh38.p12 chr9: 92,624,716-92,624,747 IPPK
    nsv3922685copy number variation1nstd102humanPathogenic GRCh38 chr9: 88,522,292-113,687,796 , NCBI36 chr9: 90,327,027-115,489,897 , GRCh37 chr9: 91,137,207-116,450,076 MUSK, LOC105376176, 464 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
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