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Items: 1 to 20 of 475

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926958copy number variation1nstd209human GRCh38 chr7: 22,163,113-22,163,220 , GRCh37.p13 chr7: 22,202,731-22,202,838 RAPGEF5
    nsv5920469copy number variation1nstd209human GRCh38 chr7: 22,129,745-22,129,841 , GRCh37.p13 chr7: 22,169,363-22,169,459 RAPGEF5
    nsv5909762copy number variation1nstd209human GRCh38 chr7: 22,161,452-22,161,501 , GRCh37.p13 chr7: 22,201,070-22,201,119 RAPGEF5
    nsv5909305copy number variation1nstd209human GRCh38 chr7: 22,268,182-22,268,234 , GRCh37.p13 chr7: 22,307,801-22,307,853 RAPGEF5
    nsv5685207mobile element insertion1nstd211human GRCh38 chr7: 22,188,331-22,188,331 , GRCh37.p13 chr7: 22,227,949-22,227,949 RAPGEF5
    nsv5684853mobile element insertion1nstd211human GRCh38 chr7: 22,254,030-22,254,030 , GRCh37.p13 chr7: 22,293,649-22,293,649 RAPGEF5
    nsv5674690mobile element insertion1nstd211human GRCh38 chr7: 22,211,123-22,211,123 , GRCh37.p13 chr7: 22,250,742-22,250,742 RAPGEF5
    nsv5582455copy number variation1nstd207human GRCh38 chr7: 22,163,113-22,163,220 , GRCh37.p13 chr7: 22,202,731-22,202,838 RAPGEF5
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5472040copy number variation1nstd206human GRCh38 chr7: 22,163,158-22,163,221 , GRCh37.p13 chr7: 22,202,776-22,202,839 RAPGEF5
    nsv5471102copy number variation1nstd206human GRCh38 chr7: 22,103,323-22,505,243 , GRCh37.p13 chr7: 22,142,941-22,544,862 , 3 more genes
    nsv5470445copy number variation1nstd206human GRCh38 chr7: 22,266,049-22,266,108 , GRCh37.p13 chr7: 22,305,668-22,305,727 RAPGEF5
    nsv5465259copy number variation1nstd206human GRCh38 chr7: 22,304,429-22,304,920 , GRCh37.p13 chr7: 22,344,048-22,344,539 RAPGEF5
    nsv5460771copy number variation1nstd206human GRCh38 chr7: 22,354,650-22,354,926 , GRCh37.p13 chr7: 22,394,269-22,394,545 RAPGEF5
    nsv5459851copy number variation1nstd206human GRCh38 chr7: 22,215,002-22,215,846 , GRCh37.p13 chr7: 22,254,621-22,255,465 , RAPGEF5
    nsv5457036copy number variation1nstd206human GRCh38 chr7: 22,171,426-22,172,279 , GRCh37.p13 chr7: 22,211,044-22,211,897 RAPGEF5
    nsv5406046mobile element insertion1nstd206human GRCh38 chr7: 22,211,123-22,211,174 , GRCh37.p13 chr7: 22,250,742-22,250,793 RAPGEF5
    nsv5399087mobile element insertion1nstd206human GRCh38 chr7: 22,254,030-22,254,081 , GRCh37.p13 chr7: 22,293,649-22,293,700 RAPGEF5
    nsv5330008translocation1nstd200human GRCh37 chr7: 22,202,776-22,202,776 , GRCh37 chr7: 22,202,839-22,202,839 , GRCh38.p12 chr7: 22,163,221-22,163,221 , GRCh38.p12 chr7: 22,163,158-22,163,158 RAPGEF5
    nsv5318629copy number variation1nstd204human GRCh37.p13 chr7: 22,254,687-22,255,480 , GRCh38.p13 chr7: 22,215,068-22,215,861 , RAPGEF5
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