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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5856503copy number variation1nstd209human GRCh38 chr9: 104,608,966-104,617,977 , GRCh37.p13 chr9: 107,371,247-107,380,258 OR13C9
    nsv5850445copy number variation1nstd209human GRCh38 chr9: 104,608,466-104,616,250 , GRCh37.p13 chr9: 107,370,747-107,378,531 OR13C9
    nsv5490651copy number variation1nstd206human GRCh38 chr9: 104,605,038-104,618,552 , GRCh37.p13 chr9: 107,367,319-107,380,833 OR13C9, OR13C2
    nsv5488186copy number variation1nstd206human GRCh38 chr9: 104,606,000-104,618,552 , GRCh37.p13 chr9: 107,368,281-107,380,833 OR13C2, OR13C9
    nsv5259786copy number variation1nstd204human GRCh38.p13 chr9: 104,614,451-104,617,977 , GRCh37.p13 chr9: 107,376,732-107,380,258 OR13C9
    nsv5248779copy number variation1nstd204human GRCh38.p13 chr9: 104,605,340-104,617,194 , GRCh37.p13 chr9: 107,367,621-107,379,475 OR13C9, OR13C2
    nsv5248653copy number variation1nstd204human GRCh38.p13 chr9: 104,604,812-104,618,079 , GRCh37.p13 chr9: 107,367,093-107,380,360 OR13C9, OR13C2
    nsv5248209copy number variation1nstd204human GRCh38.p13 chr9: 104,605,341-104,617,927 , GRCh37.p13 chr9: 107,367,622-107,380,208 OR13C9, OR13C2
    nsv5248166copy number variation1nstd204human GRCh38.p13 chr9: 104,605,301-104,618,000 , GRCh37.p13 chr9: 107,367,582-107,380,281 OR13C2, OR13C9
    nsv5246843copy number variation1nstd204human GRCh38.p13 chr9: 104,613,301-104,618,100 , GRCh37.p13 chr9: 107,375,582-107,380,381 OR13C9
    nsv5246277copy number variation1nstd204human GRCh38.p13 chr9: 104,605,301-104,619,600 , GRCh37.p13 chr9: 107,367,582-107,381,881 OR13C2, OR13C9
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4679196copy number variation1nstd189human GRCh37.p13 chr9: 107,061,882-107,737,966 , GRCh38.p12 chr9: 104,299,601-104,975,685 ABCA1, NIPSNAP3A, 18 more genes
    nsv4610934copy number variation1nstd183human GRCh37 chr9: 107,366,951-107,379,528 , GRCh38.p12 chr9: 104,604,670-104,617,247 OR13C9, OR13C2
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455409copy number variation1nstd102humanUncertain significance GRCh37 chr9: 106,618,735-107,897,515 , GRCh38.p12 chr9: 103,856,454-105,135,234 LOC107987105, OR13D1, 27 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
    nsv4428879copy number variation1nstd174human GRCh37 chr9: 107,363,821-107,381,569 , GRCh38.p12 chr9: 104,601,540-104,619,288 OR13C2, OR13C9
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
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