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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148263copy number variation1nstd102humanPathogenic GRCh38 chr9: 102,995,214-108,903,040 , GRCh37.p13 chr9: 105,757,496-111,665,320 ACTL7B, OR13C3, 88 more genes
    nsv7074978inversion1nstd229human GRCh38 chr9: 106,755,903-108,407,110 , GRCh37.p13 chr9: 109,518,184-111,169,390 LOC105376209, LINC01509, 31 more genes
    nsv6865890copy number variation1nstd229human GRCh38 chr9: 107,880,214-107,969,076 , GRCh37.p13 chr9: 110,642,495-110,731,357 RPS15AP27, RNA5SP293
    nsv6862861copy number variation1nstd229human GRCh38 chr9: 107,936,601-108,176,008 , GRCh37.p13 chr9: 110,698,882-110,938,288 CHCHD4P2, RPL31P43, 4 more genes
    nsv6859394copy number variation1nstd229human GRCh38 chr9: 107,961,503-107,965,994 , GRCh37.p13 chr9: 110,723,784-110,728,275 RPS15AP27
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6448332copy number variation1nstd223human GRCh38 chr9: 107,891,904-107,970,809 , GRCh37.p13 chr9: 110,654,185-110,733,090 RNA5SP293, RPS15AP27
    nsv6439383copy number variation1nstd223human GRCh38 chr9: 107,962,806-107,962,910 , GRCh37.p13 chr9: 110,725,087-110,725,191 RPS15AP27
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314062copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 109,265,628-117,650,999 , GRCh38.p12 chr9: 106,503,347-114,888,719 ALAD, AMBP, 151 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6267758copy number variation1nstd214human GRCh38 chr9: 107,962,866-107,962,969 , GRCh37.p13 chr9: 110,725,147-110,725,250 , RPS15AP27
    nsv6137424copy number variation1nstd213human GRCh37 chr9: 110,640,000-111,410,001 , GRCh38.p12 chr9: 107,877,719-108,647,721 RPL36P14, RPL31P43, 7 more genes
    nsv6137327copy number variation1nstd213human GRCh37 chr9: 109,340,000-112,470,001 , GRCh38.p12 chr9: 106,577,719-109,707,721 ACTL7A, TMEM245, 55 more genes
    nsv6136634copy number variation1nstd213human GRCh37 chr9: 110,630,000-111,060,001 , GRCh38.p12 chr9: 107,867,719-108,297,721 RPL31P43, CHCHD4P2, 6 more genes
    nsv5925499copy number variation1nstd209human GRCh38 chr9: 107,962,806-107,962,909 , GRCh37.p13 chr9: 110,725,087-110,725,190 , RPS15AP27
    nsv5603039copy number variation1nstd207human GRCh38 chr9: 107,962,806-107,962,909 , GRCh37.p13 chr9: 110,725,087-110,725,190 , RPS15AP27
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4729397copy number variation1nstd102humanUncertain significance GRCh37 chr9: 110,273,670-111,717,897 , GRCh38.p12 chr9: 107,511,389-108,955,617 RN7SL659P, LOC105376207, 25 more genes
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