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Items: 1 to 20 of 277

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130841insertion1nstd186human GRCh37 chr19: 3,145,581-3,145,581 , GRCh38.p12 chr19: 3,145,583-3,145,583 GNA15-DT, GNA15
    nsv5978410insertion1nstd209human GRCh38 chr19: 3,135,839-3,135,839 , GRCh37.p13 chr19: 3,135,837-3,135,837 GNA15
    nsv5978294insertion1nstd209human GRCh38 chr19: 3,145,577-3,145,577 , GRCh37.p13 chr19: 3,145,575-3,145,575 GNA15-DT, GNA15
    nsv5972142insertion1nstd209human GRCh38 chr19: 3,140,044-3,140,044 , GRCh37.p13 chr19: 3,140,042-3,140,042 GNA15, GNA15-DT
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5944186copy number variation1nstd209human GRCh38 chr19: 3,154,563-3,154,649 , GRCh37.p13 chr19: 3,154,561-3,154,647 GNA15-DT, GNA15
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5936434copy number variation1nstd209human GRCh38 chr19: 3,149,256-3,149,313 , GRCh37.p13 chr19: 3,149,254-3,149,311 GNA15-DT, GNA15
    nsv5935865copy number variation1nstd209human GRCh38 chr19: 3,157,250-3,165,421 , GRCh37.p13 chr19: 3,157,248-3,165,419 GNA15
    nsv5933475copy number variation1nstd209human GRCh38 chr19: 3,144,696-3,145,020 , GRCh37.p13 chr19: 3,144,694-3,145,018 GNA15-DT, GNA15
    nsv5873442copy number variation1nstd209human GRCh38 chr19: 3,157,158-3,165,564 , GRCh37.p13 chr19: 3,157,156-3,165,562 GNA15
    nsv5728814mobile element insertion1nstd211human GRCh38 chr19: 3,158,947-3,158,947 , GRCh37.p13 chr19: 3,158,945-3,158,945 GNA15
    nsv5661058insertion1nstd207human GRCh38 chr19: 3,145,577-3,145,577 , GRCh37.p13 chr19: 3,145,575-3,145,575 GNA15, GNA15-DT
    nsv5648675insertion1nstd207human GRCh38 chr19: 3,154,563-3,154,563 , GRCh37.p13 chr19: 3,154,561-3,154,561 GNA15, GNA15-DT
    nsv5600027copy number variation1nstd207human GRCh38 chr19: 3,154,563-3,154,649 , GRCh37.p13 chr19: 3,154,561-3,154,647 GNA15-DT, GNA15
    nsv5558340sequence alteration1nstd206human GRCh38 chr19: 3,144,551-3,144,705 , GRCh37.p13 chr19: 3,144,549-3,144,703 GNA15, GNA15-DT
    nsv5552623insertion1nstd206human GRCh38 chr19: 3,145,583-3,145,583 , GRCh37.p13 chr19: 3,145,581-3,145,581 GNA15, GNA15-DT
    nsv5530434copy number variation1nstd206human GRCh38 chr19: 3,141,402-3,145,615 , GRCh37.p13 chr19: 3,141,400-3,145,613 GNA15-DT, GNA15
    nsv5527692copy number variation1nstd206human GRCh38 chr19: 3,147,059-3,147,135 , GRCh37.p13 chr19: 3,147,057-3,147,133 GNA15-DT, GNA15
    nsv5323950copy number variation1nstd204human GRCh37.p13 chr19: 3,150,682-3,150,823 , GRCh38.p13 chr19: 3,150,684-3,150,825 GNA15-DT, GNA15
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