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Items: 1 to 20 of 298

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv6938012copy number variation1nstd229human GRCh38 chr12: 28,737,101-28,739,800 , GRCh37.p13 chr12: 28,890,034-28,892,733 LOC105369711
    nsv6936872copy number variation1nstd229human GRCh38 chr12: 28,726,218-28,736,176 , GRCh37.p13 chr12: 28,879,151-28,889,109 LOC105369711
    nsv6935369copy number variation1nstd229human GRCh38 chr12: 28,707,941-28,716,266 , GRCh37.p13 chr12: 28,860,874-28,869,199 LOC105369711
    nsv6934980copy number variation1nstd229human GRCh38 chr12: 28,758,579-28,758,591 , GRCh37.p13 chr12: 28,911,512-28,911,524 LOC105369711
    nsv6934778copy number variation1nstd229human GRCh38 chr12: 28,791,577-28,794,599 , GRCh37.p13 chr12: 28,944,510-28,947,532 LOC105369711
    nsv6934386copy number variation1nstd229human GRCh38 chr12: 28,791,194-28,827,316 , GRCh37.p13 chr12: 28,944,127-28,980,249 LOC105369711
    nsv6934317copy number variation1nstd229human GRCh38 chr12: 28,734,632-28,740,212 , GRCh37.p13 chr12: 28,887,565-28,893,145 LOC105369711
    nsv6932955copy number variation1nstd229human GRCh38 chr12: 28,769,018-28,771,934 , GRCh37.p13 chr12: 28,921,951-28,924,867 LOC105369711
    nsv6931076copy number variation1nstd229human GRCh38 chr12: 28,751,701-28,766,100 , GRCh37.p13 chr12: 28,904,634-28,919,033 LOC105369711
    nsv6923194copy number variation1nstd229human GRCh38 chr12: 28,735,286-28,739,418 , GRCh37.p13 chr12: 28,888,219-28,892,351 LOC105369711
    nsv6922870copy number variation1nstd229human GRCh38 chr12: 28,772,125-28,779,919 , GRCh37.p13 chr12: 28,925,058-28,932,852 LOC105369711
    nsv6922169copy number variation1nstd229human GRCh38 chr12: 28,751,801-28,758,700 , GRCh37.p13 chr12: 28,904,734-28,911,633 LOC105369711
    nsv6920927copy number variation1nstd229human GRCh38 chr12: 28,789,270-28,795,700 , GRCh37.p13 chr12: 28,942,203-28,948,633 LOC105369711
    nsv6918534copy number variation1nstd229human GRCh38 chr12: 28,759,136-29,359,851 , GRCh37.p13 chr12: 28,912,069-29,512,784 LOC101928735, LOC100506606, 3 more genes
    nsv6637881copy number variation1nstd102humanUncertain significance GRCh37 chr12: 28,911,901-29,518,739 , GRCh38.p12 chr12: 28,758,968-29,365,806 LOC101928735, LOC100506606, 3 more genes
    nsv6475021copy number variation1nstd223human GRCh38 chr12: 28,720,695-28,777,899 , GRCh37.p13 chr12: 28,873,628-28,930,832 LOC105369711
    nsv6470709copy number variation1nstd223human GRCh38 chr12: 28,707,401-28,716,500 , GRCh37.p13 chr12: 28,860,334-28,869,433 LOC105369711
    nsv6467916copy number variation1nstd223human GRCh38 chr12: 28,734,632-28,740,212 , GRCh37.p13 chr12: 28,887,565-28,893,145 LOC105369711
    nsv6463804copy number variation1nstd223human GRCh38 chr12: 28,743,589-28,744,031 , GRCh37.p13 chr12: 28,896,522-28,896,964 LOC105369711
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