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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7065644inversion1nstd229human GRCh38 chr20: 59,198,359-59,198,378 , GRCh37.p13 chr20: 57,773,414-57,773,433 ZNF831
    nsv7064434inversion1nstd229human GRCh38 chr20: 59,224,297-59,230,929 , GRCh37.p13 chr20: 57,799,352-57,805,984 ZNF831
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7035956copy number variation1nstd229human GRCh38 chr20: 59,210,856-59,211,065 , GRCh37.p13 chr20: 57,785,911-57,786,120 ZNF831
    nsv7034469copy number variation1nstd229human GRCh38 chr20: 59,212,651-59,213,225 , GRCh37.p13 chr20: 57,787,706-57,788,280 ZNF831
    nsv7032537copy number variation1nstd229human GRCh38 chr20: 59,162,131-59,163,004 , GRCh37.p13 chr20: 57,737,186-57,738,059 ZNF831
    nsv7030219copy number variation1nstd229human GRCh38 chr20: 59,166,552-59,172,419 , GRCh37.p13 chr20: 57,741,607-57,747,474 ZNF831
    nsv7028313copy number variation1nstd229human GRCh38 chr20: 59,243,647-59,247,509 , GRCh37.p13 chr20: 57,818,702-57,822,564 ZNF831
    nsv7028000copy number variation1nstd229human GRCh38 chr20: 59,227,251-59,230,449 , GRCh37.p13 chr20: 57,802,306-57,805,504 ZNF831
    nsv7024487copy number variation1nstd229human GRCh38 chr20: 59,213,474-59,213,641 , GRCh37.p13 chr20: 57,788,529-57,788,696 ZNF831
    nsv7021712copy number variation1nstd229human GRCh38 chr20: 59,153,624-59,153,682 , GRCh37.p13 chr20: 57,728,679-57,728,737 ZNF831
    nsv6597835inversion1nstd223human GRCh38 chr20: 59,172,197-59,173,370 , GRCh37.p13 chr20: 57,747,252-57,748,425 ZNF831
    nsv6597499inversion1nstd223human GRCh38 chr20: 59,239,598-59,240,530 , GRCh37.p13 chr20: 57,814,653-57,815,585 ZNF831
    nsv6595601inversion1nstd223human GRCh38 chr20: 59,239,710-59,240,551 , GRCh37.p13 chr20: 57,814,765-57,815,606 ZNF831
    nsv6553003copy number variation1nstd223human GRCh38 chr20: 59,243,647-59,247,509 , GRCh37.p13 chr20: 57,818,702-57,822,564 ZNF831
    nsv6551002copy number variation1nstd223human GRCh38 chr20: 59,179,394-59,179,854 , GRCh37.p13 chr20: 57,754,449-57,754,909 ZNF831
    nsv6540259copy number variation1nstd223human GRCh38 chr20: 59,153,623-59,153,682 , GRCh37.p13 chr20: 57,728,678-57,728,737 ZNF831
    nsv6539400copy number variation1nstd223human GRCh38 chr20: 59,213,182-59,214,636 , GRCh37.p13 chr20: 57,788,237-57,789,691 ZNF831
    nsv6314208copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202 LOC105372698, LOC105372695, 176 more genes
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