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Items: 1 to 20 of 3666

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127357insertion1nstd186human GRCh37 chr4: 182,427,929-182,427,934 , GRCh38.p12 chr4: 181,506,776-181,506,781 TENM3
    nsv6117059mobile element insertion1nstd186human GRCh37 chr4: 183,300,772-183,300,823 , GRCh38.p12 chr4: 182,379,619-182,379,670 TENM3
    nsv5979718inversion1nstd209human GRCh38 chr4: 182,650,937-182,650,996 , GRCh37.p13 chr4: 183,572,090-183,572,149 TENM3
    nsv5967553insertion1nstd209human GRCh38 chr4: 182,253,955-182,253,955 , GRCh37.p13 chr4: 183,175,108-183,175,108 TENM3
    nsv5966476insertion1nstd209human GRCh38 chr4: 181,856,034-181,856,034 , GRCh37.p13 chr4: 182,777,187-182,777,187 TENM3
    nsv5965236insertion1nstd209human GRCh38 chr4: 182,299,016-182,299,016 , GRCh37.p13 chr4: 183,220,169-183,220,169 TENM3
    nsv5961674insertion1nstd209human GRCh38 chr4: 182,156,680-182,156,680 , GRCh37.p13 chr4: 183,077,833-183,077,833 TENM3
    nsv5961148insertion1nstd209human GRCh38 chr4: 182,627,630-182,627,630 , GRCh37.p13 chr4: 183,548,783-183,548,783 TENM3
    nsv5959816insertion1nstd209human GRCh38 chr4: 181,525,396-181,525,396 , GRCh37.p13 chr4: 182,446,549-182,446,549 TENM3
    nsv5956623insertion1nstd209human GRCh38 chr4: 182,161,628-182,161,628 , GRCh37.p13 chr4: 183,082,781-183,082,781 TENM3
    nsv5956466insertion1nstd209human GRCh38 chr4: 182,379,604-182,379,604 , GRCh37.p13 chr4: 183,300,757-183,300,757 TENM3
    nsv5954308insertion1nstd209human GRCh38 chr4: 181,473,757-181,473,757 , GRCh37.p13 chr4: 182,394,910-182,394,910 TENM3
    nsv5953592insertion1nstd209human GRCh38 chr4: 181,467,083-181,467,083 , GRCh37.p13 chr4: 182,388,236-182,388,236 TENM3
    nsv5953355insertion1nstd209human GRCh38 chr4: 182,426,007-182,426,007 , GRCh37.p13 chr4: 183,347,160-183,347,160 TENM3
    nsv5952954insertion1nstd209human GRCh38 chr4: 181,605,584-181,605,584 , GRCh37.p13 chr4: 182,526,737-182,526,737 TENM3
    nsv5952215insertion1nstd209human GRCh38 chr4: 182,101,188-182,101,188 , GRCh37.p13 chr4: 183,022,341-183,022,341 TENM3
    nsv5948426insertion1nstd209human GRCh38 chr4: 182,228,374-182,228,374 , GRCh37.p13 chr4: 183,149,527-183,149,527 TENM3
    nsv5947689insertion1nstd209human GRCh38 chr4: 182,777,543-182,777,543 , GRCh37.p13 chr4: 183,698,696-183,698,696 TENM3
    nsv5906640copy number variation1nstd209human GRCh38 chr4: 181,473,782-181,473,868 , GRCh37.p13 chr4: 182,394,935-182,395,021 TENM3
    nsv5904267copy number variation1nstd209human GRCh38 chr4: 182,000,745-182,000,838 , GRCh37.p13 chr4: 182,921,898-182,921,991 TENM3
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