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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5889985copy number variation1nstd209human GRCh38 chr4: 119,210,350-119,211,833 , GRCh37.p13 chr4: 120,131,505-120,132,988 LOC101929762, USP53
    nsv5837328copy number variation1nstd209human GRCh38 chr4: 119,210,375-119,211,874 , GRCh37.p13 chr4: 120,131,530-120,133,029 LOC101929762, USP53
    nsv5684158mobile element insertion1nstd211human GRCh38 chr4: 119,260,042-119,260,042 , GRCh37.p13 chr4: 120,181,197-120,181,197 USP53
    nsv5678042mobile element insertion1nstd211human GRCh38 chr4: 119,214,138-119,214,138 , GRCh37.p13 chr4: 120,135,293-120,135,293 USP53
    nsv5615357insertion1nstd207human GRCh38 chr4: 119,213,660-119,213,660 , GRCh37.p13 chr4: 120,134,815-120,134,815 USP53
    nsv5567552copy number variation1nstd207human GRCh38 chr4: 119,248,243-119,248,446 , GRCh37.p13 chr4: 120,169,398-120,169,601 USP53
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5549305insertion1nstd206human GRCh38 chr4: 119,213,673-119,213,694 , GRCh37.p13 chr4: 120,134,828-120,134,849 USP53
    nsv5469036copy number variation1nstd206human GRCh38 chr4: 119,248,376-119,248,641 , GRCh37.p13 chr4: 120,169,531-120,169,796 USP53
    nsv5466719copy number variation1nstd206human GRCh38 chr4: 119,210,353-119,211,834 , GRCh37.p13 chr4: 120,131,508-120,132,989 USP53, LOC101929762
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 more genes
    nsv5347055translocation1nstd200human GRCh38 chr4: 119,293,398-119,293,398 , GRCh38 chr4: 119,293,458-119,293,458 , GRCh37.p13 chr4: 120,214,553-120,214,553 , GRCh37.p13 chr4: 120,214,613-120,214,613 USP53
    nsv5347054translocation1nstd200human GRCh38 chr4: 119,210,460-119,210,460 , GRCh38 chr4: 119,211,802-119,211,802 , GRCh37.p13 chr4: 120,132,957-120,132,957 , GRCh37.p13 chr4: 120,131,615-120,131,615 USP53, LOC101929762
    nsv5230306copy number variation1nstd204human GRCh38.p13 chr4: 119,278,297-119,283,880 , GRCh37.p13 chr4: 120,199,452-120,205,035 USP53
    nsv5089387mobile element insertion1nstd203human GRCh38 chr4: 119,262,832-119,262,844 , GRCh37.p13 chr4: 120,183,987-120,183,999 USP53
    nsv5084688mobile element insertion1nstd203human GRCh38 chr4: 119,284,577-119,284,589 , GRCh37.p13 chr4: 120,205,732-120,205,744 USP53
    nsv4935547copy number variation1nstd200human GRCh38 chr4: 119,231,387-119,234,811 , GRCh37.p13 chr4: 120,152,542-120,155,966 USP53
    nsv4808192copy number variation1nstd200human GRCh37 chr4: 120,131,508-120,132,989 , GRCh38.p12 chr4: 119,210,353-119,211,834 USP53, LOC101929762
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
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