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Items: 1 to 20 of 328

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7137132copy number variation1nstd102humanUncertain significance GRCh37 chr17: 65,445-695,309 , GRCh38.p12 chr17: 215,654-792,069 RPS4XP17, RFLNB, 11 more genes
    nsv7098885copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1-450,099 , GRCh38.p12 chr17|NW_003315952.3: 90,208-375,691 , GRCh38.p12 chr17: 150,208-546,859 LINC02091, VPS53, 8 more genes
    nsv7070813inversion1nstd229human GRCh38 chr17: 181,363-638,312 , GRCh37.p13 chr17|NW_003315952.2: 31,154-270,261 , GRCh37.p13 chr17: 67,876-296,626 RFLNB, LOC105371425, 7 more genes
    nsv7070618inversion1nstd229human GRCh38 chr17: 426,050-796,506 , GRCh37.p13 chr17: 396,627-699,746 GEMIN4, MRM3, 6 more genes
    nsv6997054copy number variation1nstd229human GRCh38 chr17: 383,818-640,526 , GRCh37.p13 chr17: 396,627-543,766 RFLNB, LIAT1, 2 more genes
    nsv6995849copy number variation1nstd229human GRCh38 chr17: 426,628-969,586 , GRCh37.p13 chr17: 396,627-872,826 VPS53, MRM3, 8 more genes
    nsv6995636copy number variation1nstd229human GRCh38 chr17: 436,101-439,800 , GRCh37.p13 chr17|NW_003315951.1: 33,464-37,163 , GRCh37.p13 chr17: 285,892-289,591 RFLNB
    nsv6994909copy number variation1nstd229human GRCh38 chr17: 338,200-588,056 , GRCh37.p13 chr: NaN-NaN VPS53, LOC105371430, 4 more genes
    nsv6992669copy number variation1nstd229human GRCh38 chr17: 152,803-735,816 , GRCh37.p13 chr17: 5,326-639,056 DOC2B, RPS4XP17, 9 more genes
    nsv6991988copy number variation1nstd229human GRCh38 chr17: 251,815-1,065,942 , GRCh37.p13 chr17: 396,627-969,182 LIAT1, RPS4XP17, 17 more genes
    nsv6988554copy number variation1nstd229human GRCh38 chr17: 301,576-970,376 , GRCh37.p13 chr17: 396,627-873,616 RPS4XP17, RFLNB, 13 more genes
    nsv6988314copy number variation1nstd229human GRCh38 chr17: 417,295-440,429 , GRCh37.p13 chr17: 267,086-290,220 , GRCh37.p13 chr17|NW_003315951.1: 14,658-37,792 RFLNB
    nsv6988301copy number variation1nstd229human GRCh38 chr17: 252,976-780,682 , GRCh37.p13 chr17: 396,627-683,922 MRM3, LOC105371430, 11 more genes
    nsv6987278copy number variation1nstd229human GRCh38 chr17: 283,116-441,583 , GRCh37.p13 chr17|NW_004070872.2: 223,114-342,635 LOC105371430, LIAT1, 4 more genes
    nsv6983179copy number variation1nstd229human GRCh38 chr17: 277,729-847,794 , GRCh37.p13 chr17: 396,627-751,034 MRM3, LOC105371430, 12 more genes
    nsv6979822copy number variation1nstd229human GRCh38 chr17: 365,103-608,879 , GRCh37.p13 chr: NaN-NaN LOC105371430, VPS53, 2 more genes
    nsv6979723copy number variation1nstd229human GRCh38 chr17: 417,542-438,581 , GRCh37.p13 chr17: 267,333-288,372 , GRCh37.p13 chr17|NW_003315951.1: 14,905-35,944 RFLNB
    nsv6637505copy number variation1nstd102humanPathogenic GRCh37 chr17: 526-1,690,452 , GRCh38.p12 chr17: 150,733-1,787,158 RPS4XP17, LIAT1, 43 more genes
    nsv6624293copy number variation1nstd224human GRCh37 chr17: 53,011-1,082,126 , GRCh38.p12 chr17: 203,220-1,178,832 ABR, TIMM22, 20 more genes
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