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Items: 1 to 20 of 601

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139709insertion1nstd232human GRCh37.p13 chr12: 120,201,092-120,201,092 , GRCh38.p12 chr12: 119,763,288-119,763,288 CIT
    nsv7070130inversion1nstd229human GRCh38 chr12: 119,778,006-119,781,324 , GRCh37.p13 chr12: 120,215,810-120,219,128 CIT
    nsv7066447inversion1nstd229human GRCh38 chr12: 119,852,571-119,855,853 , GRCh37.p13 chr12: 120,290,375-120,293,657 CIT
    nsv7062660inversion1nstd229human GRCh38 chr12: 119,747,908-119,748,019 , GRCh37.p13 chr12: 120,185,713-120,185,824 CIT
    nsv6937948copy number variation1nstd229human GRCh38 chr12: 119,509,138-119,753,809 , GRCh37.p13 chr12: 119,946,943-120,191,613 PRKAB1, MIR1178, 5 more genes
    nsv6935933copy number variation1nstd229human GRCh38 chr12: 119,682,121-119,684,246 , GRCh37.p13 chr12: 120,119,926-120,122,051 CIT, PRKAB1
    nsv6930380copy number variation1nstd229human GRCh38 chr12: 119,814,638-119,817,839 , GRCh37.p13 chr12: 120,252,442-120,255,643 CIT
    nsv6930001copy number variation1nstd229human GRCh38 chr12: 119,839,518-119,841,973 , GRCh37.p13 chr12: 120,277,322-120,279,777 CIT
    nsv6926542copy number variation1nstd229human GRCh38 chr12: 119,872,352-119,877,307 , GRCh37.p13 chr12: 120,310,156-120,315,111 CIT
    nsv6925970copy number variation1nstd229human GRCh38 chr12: 119,790,463-119,790,507 , GRCh37.p13 chr12: 120,228,267-120,228,311 CIT
    nsv6925037copy number variation1nstd229human GRCh38 chr12: 119,872,909-119,884,841 , GRCh37.p13 chr12: 120,310,713-120,322,645 CIT
    nsv6924204copy number variation1nstd229human GRCh38 chr12: 119,858,690-119,862,384 , GRCh37.p13 chr12: 120,296,494-120,300,188 CIT
    nsv6922503copy number variation1nstd229human GRCh38 chr12: 119,818,476-119,820,496 , GRCh37.p13 chr12: 120,256,280-120,258,300 CIT
    nsv6922403copy number variation1nstd229human GRCh38 chr12: 119,694,354-119,695,040 , GRCh37.p13 chr12: 120,132,159-120,132,845 CIT
    nsv6919994copy number variation1nstd229human GRCh38 chr12: 119,731,406-119,731,437 , GRCh37.p13 chr12: 120,169,211-120,169,242 CIT
    nsv6919911copy number variation1nstd229human GRCh38 chr12: 119,862,044-119,863,635 , GRCh37.p13 chr12: 120,299,848-120,301,439 CIT
    nsv6590036inversion1nstd223human GRCh38 chr12: 119,731,116-119,731,839 , GRCh37.p13 chr12: 120,168,921-120,169,644 CIT
    nsv6588723inversion1nstd223human GRCh38 chr12: 119,811,310-119,811,967 , GRCh37.p13 chr12: 120,249,114-120,249,771 CIT
    nsv6587306inversion1nstd223human GRCh38 chr12: 119,862,020-119,862,592 , GRCh37.p13 chr12: 120,299,824-120,300,396 CIT
    nsv6584216inversion1nstd223human GRCh38 chr12: 119,843,764-119,844,142 , GRCh37.p13 chr12: 120,281,568-120,281,946 CIT
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