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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5856631copy number variation2nstd209human GRCh38 chr9: 92,315,767-92,316,766 , GRCh37.p13 chr9: 95,078,049-95,079,048 NOL8
    nsv5673969copy number variation1nstd102humanPathogenic GRCh37 chr9: 95,007,241-95,237,179 , GRCh38.p12 chr9: 92,244,959-92,474,897 IARS1, OMD, 7 more genes
    nsv5562344sequence alteration1nstd206human GRCh38 chr9: 92,266,854-92,881,037 , GRCh37.p13 chr9: 95,029,136-95,643,319 ECM2, BICD2, 21 more genes
    nsv5533932insertion1nstd206human GRCh38 chr9: 92,312,720-92,312,770 , GRCh37.p13 chr9: 95,075,002-95,075,052 NOL8
    nsv5132799mobile element insertion1nstd203human GRCh38 chr9: 92,305,567-92,305,582 , GRCh37.p13 chr9: 95,067,849-95,067,864 NOL8
    nsv4974699copy number variation1nstd200human GRCh38 chr9: 91,924,473-92,376,273 , GRCh37.p13 chr9: 94,686,755-95,138,555 , RPL21P82, 21 more genes
    nsv4973179copy number variation1nstd200human GRCh38 chr9: 92,263,835-92,332,085 , GRCh37.p13 chr9: 95,026,117-95,094,367 SNORA84, MIR3651, 3 more genes
    nsv4887530inversion1nstd200human GRCh37 chr9: 90,662,371-96,951,001 , GRCh38.p12 chr9: 88,047,456-94,188,719 , MTATP6P29, 125 more genes
    nsv4814856copy number variation1nstd200human GRCh37 chr9: 94,686,755-95,138,555 , GRCh38.p12 chr9: 91,924,473-92,376,273 , SNORA84, 21 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
    nsv4490140mobile element insertion1nstd166human GRCh37.p13 chr9: 95,066,364-95,066,364 , GRCh38.p12 chr9: 92,304,082-92,304,082 NOL8
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 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
    nsv4418188copy number variation1nstd174human GRCh37 chr9: 95,057,462-95,141,947 , GRCh38.p12 chr9: 92,295,180-92,379,665 NOL8, CENPP, 1 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
    nsv4185339copy number variation1nstd166human GRCh37.p13 chr9: 95,071,859-95,071,953 , GRCh38.p12 chr9: 92,309,577-92,309,671 NOL8
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