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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963580insertion1nstd209human GRCh38 chr5: 34,717,925-34,717,925 , GRCh37.p13 chr5: 34,718,030-34,718,030 RAI14
    nsv5960779insertion1nstd209human GRCh38 chr5: 34,754,524-34,754,524 , GRCh37.p13 chr5: 34,754,629-34,754,629 RAI14
    nsv5957979insertion1nstd209human GRCh38 chr5: 34,752,726-34,752,726 , GRCh37.p13 chr5: 34,752,831-34,752,831 RAI14
    nsv5957381insertion1nstd209human GRCh38 chr5: 34,665,007-34,665,007 , GRCh37.p13 chr5: 34,665,112-34,665,112 RAI14
    nsv5907090copy number variation1nstd209human GRCh38 chr5: 34,824,913-34,825,243 , GRCh37.p13 chr5: 34,825,018-34,825,348 RAI14
    nsv5898349copy number variation1nstd209human GRCh38 chr5: 34,665,007-34,665,056 , GRCh37.p13 chr5: 34,665,112-34,665,161 RAI14
    nsv5892835copy number variation1nstd209human GRCh38 chr5: 34,710,799-34,711,299 , GRCh37.p13 chr5: 34,710,904-34,711,404 RAI14
    nsv5888275copy number variation1nstd209human GRCh38 chr5: 34,753,596-34,753,729 , GRCh37.p13 chr5: 34,753,701-34,753,834 RAI14
    nsv5718948mobile element insertion1nstd211human GRCh38 chr5: 34,825,008-34,825,008 , GRCh37.p13 chr5: 34,825,113-34,825,113 RAI14
    nsv5682685mobile element insertion2nstd211human GRCh38 chr5: 34,717,939-34,717,939 , GRCh37.p13 chr5: 34,718,044-34,718,044 RAI14
    nsv5678230mobile element insertion2nstd211human GRCh38 chr5: 34,754,513-34,754,513 , GRCh37.p13 chr5: 34,754,618-34,754,618 RAI14
    nsv5640556insertion1nstd207human GRCh38 chr5: 34,717,925-34,717,925 , GRCh37.p13 chr5: 34,718,030-34,718,030 RAI14
    nsv5634580insertion2nstd207human GRCh38 chr5: 34,665,007-34,665,007 , GRCh37.p13 chr5: 34,665,112-34,665,112 RAI14
    nsv5627646insertion1nstd207human GRCh38 chr5: 34,754,528-34,754,528 , GRCh37.p13 chr5: 34,754,633-34,754,633 RAI14
    nsv5575487copy number variation1nstd207human GRCh38 chr5: 34,665,007-34,665,056 , GRCh37.p13 chr5: 34,665,112-34,665,161 RAI14
    nsv5541232insertion1nstd206human GRCh38 chr5: 34,688,826-34,688,855 , GRCh37.p13 chr5: 34,688,931-34,688,960 RAI14
    nsv5472652copy number variation1nstd206human GRCh38 chr5: 34,558,065-35,071,637 , GRCh37.p13 chr5: 34,558,170-35,071,739 AGXT2, RAI14, 9 more genes
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5469173copy number variation1nstd206human GRCh38 chr5: 34,677,146-34,677,199 , GRCh37.p13 chr5: 34,677,251-34,677,304 RAI14
    nsv5464551copy number variation1nstd206human GRCh38 chr5: 34,710,799-34,711,206 , GRCh37.p13 chr5: 34,710,904-34,711,311 RAI14
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