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Items: 1 to 20 of 323

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131106insertion1nstd186human GRCh37 chr14: 92,247,261-92,247,302 , GRCh38.p12 chr14: 91,780,917-91,780,958 , GRCh38.p12 chr14|NT_187598.1: 248,712-248,753 TC2N
    nsv5944803copy number variation1nstd209human GRCh38 chr14: 91,824,656-91,824,713 , GRCh37.p13 chr14: 92,291,000-92,291,057 TC2N
    nsv5863782copy number variation1nstd209human GRCh38 chr14: 91,794,321-91,796,020 , GRCh37.p13 chr14: 92,260,665-92,262,364 TC2N
    nsv5857039copy number variation1nstd209human GRCh38 chr14: 91,856,737-91,857,936 , GRCh37.p13 chr14: 92,323,081-92,324,280 TC2N
    nsv5713510mobile element insertion1nstd211human GRCh38 chr14: 91,853,648-91,853,648 , GRCh37.p13 chr14: 92,319,992-92,319,992 TC2N
    nsv5712327mobile element insertion1nstd211human GRCh38 chr14: 91,788,049-91,788,049 , GRCh37.p13 chr14: 92,254,393-92,254,393 TC2N
    nsv5706846mobile element insertion1nstd211human GRCh38 chr14: 91,797,126-91,797,126 , GRCh37.p13 chr14: 92,263,470-92,263,470 TC2N
    nsv5698669mobile element insertion2nstd211human GRCh38 chr14: 91,780,917-91,780,917 , GRCh37.p13 chr14: 92,247,261-92,247,261 TC2N
    nsv5645542insertion1nstd207human GRCh38 chr14: 91,836,577-91,836,577 , GRCh37.p13 chr14: 92,302,921-92,302,921 TC2N
    nsv5547429insertion1nstd206human GRCh38 chr14: 91,780,917-91,780,958 , GRCh37.p13 chr14: 92,247,261-92,247,302 TC2N
    nsv5511516copy number variation1nstd206human GRCh38 chr14: 91,864,390-91,864,464 , GRCh37.p13 chr14: 92,330,734-92,330,808 TC2N
    nsv5508331copy number variation1nstd206human GRCh38 chr14: 91,815,919-91,816,298 , GRCh37.p13 chr14: 92,282,263-92,282,642 TC2N
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5497632copy number variation1nstd206human GRCh38 chr14: 91,850,351-91,850,415 , GRCh37.p13 chr14: 92,316,695-92,316,759 TC2N
    nsv5495110copy number variation1nstd206human GRCh38 chr14: 91,792,260-91,792,310 , GRCh37.p13 chr14: 92,258,604-92,258,654 TC2N
    nsv5493965copy number variation1nstd206human GRCh38 chr14: 91,815,387-91,816,278 , GRCh37.p13 chr14: 92,281,731-92,282,622 TC2N
    nsv5420367mobile element insertion1nstd206human GRCh38 chr14: 91,788,049-91,788,100 , GRCh37.p13 chr14: 92,254,393-92,254,444 TC2N
    nsv5274866copy number variation1nstd204human GRCh38.p13 chr14: 91,811,701-91,817,800 , GRCh37.p13 chr14: 92,278,045-92,284,144 TC2N
    nsv5267773copy number variation1nstd204human GRCh38.p13 chr14: 91,797,101-91,801,200 , GRCh37.p13 chr14: 92,263,445-92,267,544 TC2N
    nsv5262717copy number variation1nstd204human GRCh38.p13 chr14: 91,819,701-91,822,300 , GRCh37.p13 chr14: 92,286,045-92,288,644 TC2N
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