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Items: 1 to 20 of 880

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144336insertion1nstd232human GRCh37.p13 chr9: 124,733,542-124,733,542 , GRCh38.p12 chr9: 121,971,263-121,971,263 TTLL11
    nsv7143913copy number variation1nstd232human GRCh37.p13 chr9: 124,733,283-124,733,331 , GRCh38.p12 chr9: 121,971,004-121,971,052 TTLL11
    nsv7072760inversion1nstd229human GRCh38 chr9: 121,872,520-121,872,565 , GRCh37.p13 chr9: 124,634,799-124,634,844 TTLL11
    nsv7068531inversion1nstd229human GRCh38 chr9: 122,009,712-122,009,758 , GRCh37.p13 chr9: 124,771,991-124,772,037 TTLL11
    nsv7068427inversion1nstd229human GRCh38 chr9: 122,065,329-122,067,549 , GRCh37.p13 chr9: 124,827,608-124,829,828 TTLL11
    nsv7066467inversion1nstd229human GRCh38 chr9: 122,062,124-122,067,535 , GRCh37.p13 chr9: 124,824,403-124,829,814 TTLL11
    nsv6875646copy number variation1nstd229human GRCh38 chr9: 122,069,083-122,069,990 , GRCh37.p13 chr9: 124,831,362-124,832,269 TTLL11
    nsv6875478copy number variation1nstd229human GRCh38 chr9: 122,068,728-122,074,539 , GRCh37.p13 chr9: 124,831,007-124,836,818 TTLL11
    nsv6875086copy number variation1nstd229human GRCh38 chr9: 121,879,201-121,882,700 , GRCh37.p13 chr9: 124,641,480-124,644,979 TTLL11
    nsv6874908copy number variation1nstd229human GRCh38 chr9: 121,952,624-121,952,706 , GRCh37.p13 chr9: 124,714,903-124,714,985 TTLL11
    nsv6874482copy number variation1nstd229human GRCh38 chr9: 121,904,476-121,912,379 , GRCh37.p13 chr9: 124,666,755-124,674,658 TTLL11
    nsv6874232copy number variation1nstd229human GRCh38 chr9: 121,959,699-121,962,230 , GRCh37.p13 chr9: 124,721,978-124,724,509 TTLL11
    nsv6873735copy number variation1nstd229human GRCh38 chr9: 121,831,849-121,835,141 , GRCh37.p13 chr9: 124,594,128-124,597,420 TTLL11
    nsv6871239copy number variation1nstd229human GRCh38 chr9: 121,890,054-121,917,707 , GRCh37.p13 chr9: 124,652,333-124,679,986 TTLL11
    nsv6871042copy number variation1nstd229human GRCh38 chr9: 121,627,934-121,867,763 , GRCh37.p13 chr9: 124,390,213-124,630,042 LOC107987125, TTLL11, 2 more genes
    nsv6870089copy number variation1nstd229human GRCh38 chr9: 121,578,522-121,838,274 , GRCh37.p13 chr9: 124,340,801-124,600,553 DAB2IP, TTLL11, 2 more genes
    nsv6869733copy number variation1nstd229human GRCh38 chr9: 121,917,001-121,944,200 , GRCh37.p13 chr9: 124,679,280-124,706,479 TTLL11
    nsv6869677copy number variation1nstd229human GRCh38 chr9: 121,889,526-121,897,891 , GRCh37.p13 chr9: 124,651,805-124,660,170 TTLL11
    nsv6868678copy number variation1nstd229human GRCh38 chr9: 121,916,356-121,919,510 , GRCh37.p13 chr9: 124,678,635-124,681,789 TTLL11
    nsv6867345copy number variation1nstd229human GRCh38 chr9: 121,994,528-122,003,853 , GRCh37.p13 chr9: 124,756,807-124,766,132 TTLL11
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