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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5562344sequence alteration1nstd206human GRCh38 chr9: 92,266,854-92,881,037 , GRCh37.p13 chr9: 95,029,136-95,643,319 ECM2, BICD2, 21 more genes
    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
    nsv5303350copy number variation1nstd204human GRCh38.p13 chr9: 92,369,835-92,549,215 , GRCh37.p13 chr9: 95,132,117-95,311,497 ECM2, OMD, 4 more genes
    nsv5251230copy number variation1nstd204human GRCh37.p13 chr9: 95,132,183-95,311,482 , GRCh38.p13 chr9: 92,369,901-92,549,200 ECM2, OMD, 4 more genes
    nsv5248957copy number variation1nstd204human GRCh38.p13 chr9: 92,483,603-92,537,156 , GRCh37.p13 chr9: 95,245,885-95,299,438 CENPP, ECM2, 1 more genes
    nsv4973184copy number variation1nstd200human GRCh38 chr9: 92,369,860-92,549,186 , GRCh37.p13 chr9: 95,132,142-95,311,468 ECM2, OMD, 4 more genes
    nsv4887530inversion1nstd200human GRCh37 chr9: 90,662,371-96,951,001 , GRCh38.p12 chr9: 88,047,456-94,188,719 , MTATP6P29, 125 more genes
    nsv4814487copy number variation1nstd200human GRCh37 chr9: 95,132,142-95,311,468 , GRCh38.p12 chr9: 92,369,860-92,549,186 ECM2, OMD, 4 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
    nsv4676073copy number variation1nstd102humanUncertain significance GRCh37 chr9: 94,671,200-95,325,631 , GRCh38.p12 chr9: 91,908,918-92,563,349 PRSS47P, MTND3P23, 25 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
    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
    nsv4455957copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,058,076-95,292,831 , GRCh38.p12 chr9: 92,295,794-92,530,549 ECM2, LOC100420779, 6 more genes
    nsv4455714copy number variation1nstd102humanUncertain significance GRCh37 chr9: 94,667,669-95,345,847 , GRCh38.p12 chr9: 91,905,387-92,583,565 MTND4P15, SNORA84, 25 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
    nsv4190747copy number variation1nstd166human GRCh37.p13 chr9: 95,282,343-95,369,814 , GRCh38.p12 chr9: 92,520,061-92,607,532 ECM2, CENPP, 1 more genes
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