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Items: 1 to 20 of 515

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954917insertion1nstd209human GRCh38 chr5: 161,416,696-161,416,696 , GRCh37.p13 chr5: 160,843,702-160,843,702 GABRB2
    nsv5952155insertion1nstd209human GRCh38 chr5: 161,429,345-161,429,345 , GRCh37.p13 chr5: 160,856,351-160,856,351 GABRB2
    nsv5841834copy number variation2nstd209human GRCh38 chr5: 161,524,158-161,526,857 , GRCh37.p13 chr5: 160,951,164-160,953,863 GABRB2
    nsv5681072mobile element insertion1nstd211human GRCh38 chr5: 161,459,035-161,459,035 , GRCh37.p13 chr5: 160,886,041-160,886,041 GABRB2
    nsv5675964mobile element insertion1nstd211human GRCh38 chr5: 161,412,580-161,412,580 , GRCh37.p13 chr5: 160,839,586-160,839,586 GABRB2
    nsv5673662copy number variation1nstd102humanLikely benign GRCh37 chr5: 160,721,068-160,763,796 , GRCh38.p12 chr5: 161,294,061-161,336,789 GABRB2
    nsv5466701copy number variation1nstd206human GRCh38 chr5: 161,369,686-161,369,996 , GRCh37.p13 chr5: 160,796,692-160,797,002 GABRB2
    nsv5462416copy number variation1nstd206human GRCh38 chr5: 161,405,009-161,405,339 , GRCh37.p13 chr5: 160,832,015-160,832,345 GABRB2
    nsv5461879copy number variation1nstd206human GRCh38 chr5: 161,316,369-161,317,148 , GRCh37.p13 chr5: 160,743,376-160,744,155 GABRB2
    nsv5460593copy number variation1nstd206human GRCh38 chr5: 161,348,390-161,348,448 , GRCh37.p13 chr5: 160,775,397-160,775,455 GABRB2
    nsv5457129copy number variation1nstd206human GRCh38 chr5: 161,289,102-161,290,233 , GRCh37.p13 chr5: 160,716,109-160,717,240 GABRB2
    nsv5408899mobile element insertion1nstd206human GRCh38 chr5: 161,459,035-161,459,086 , GRCh37.p13 chr5: 160,886,041-160,886,092 GABRB2
    nsv5407649mobile element insertion1nstd206human GRCh38 chr5: 161,412,580-161,412,631 , GRCh37.p13 chr5: 160,839,586-160,839,637 GABRB2
    nsv5369042translocation1nstd200human GRCh38 chr5: 161,515,517-161,515,517 , GRCh38 chr5: 161,516,249-161,516,249 , GRCh37.p13 chr5: 160,942,523-160,942,523 , GRCh37.p13 chr5: 160,943,255-160,943,255 GABRB2
    nsv5362620translocation1nstd200human GRCh38 chr5: 161,497,466-161,497,466 , GRCh38 chr5: 161,497,381-161,497,381 , GRCh37.p13 chr5: 160,924,387-160,924,387 , GRCh37.p13 chr5: 160,924,472-160,924,472 GABRB2
    nsv5362619translocation1nstd200human GRCh38 chr5: 161,468,555-161,468,555 , GRCh38 chr5: 161,469,094-161,469,094 , GRCh37.p13 chr5: 160,895,561-160,895,561 , GRCh37.p13 chr5: 160,896,100-160,896,100 GABRB2
    nsv5362618translocation1nstd200human GRCh38 chr5: 161,327,584-161,327,584 , GRCh38 chr5: 161,327,681-161,327,681 , GRCh37.p13 chr5: 160,754,591-160,754,591 , GRCh37.p13 chr5: 160,754,688-160,754,688 GABRB2
    nsv5362617translocation1nstd200human GRCh38 chr5: 161,289,102-161,289,102 , GRCh38 chr5: 161,290,233-161,290,233 , GRCh37.p13 chr5: 160,716,109-160,716,109 , GRCh37.p13 chr5: 160,717,240-160,717,240 GABRB2
    nsv5345055translocation1nstd200human GRCh37 chr5: 160,943,255-160,943,255 , GRCh37 chr5: 160,942,523-160,942,523 , GRCh38.p12 chr5: 161,515,517-161,515,517 , GRCh38.p12 chr5: 161,516,249-161,516,249 GABRB2
    nsv5315817copy number variation1nstd204human GRCh38.p13 chr5: 161,548,254-161,549,997 , GRCh37.p13 chr5: 160,975,260-160,977,003 GABRB2
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