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Items: 1 to 20 of 782

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137787copy number variation1nstd102humanBenign GRCh38 chr2: 1,639,032-1,639,083 , GRCh37 chr2: 1,642,804-1,642,855 PXDN
    nsv5886963copy number variation1nstd209human GRCh38 chr2: 1,702,968-1,703,072 , GRCh37.p13 chr2: 1,706,740-1,706,844 PXDN
    nsv5884279copy number variation1nstd209human GRCh38 chr2: 1,637,846-1,637,919 , GRCh37.p13 chr2: 1,641,618-1,641,691 PXDN
    nsv5881791copy number variation1nstd209human GRCh38 chr2: 1,731,282-1,731,331 , GRCh37.p13 chr2: 1,735,054-1,735,103 PXDN
    nsv5879545copy number variation1nstd209human GRCh38 chr2: 1,715,846-1,715,910 , GRCh37.p13 chr2: 1,719,618-1,719,682 PXDN
    nsv5878135copy number variation1nstd209human GRCh38 chr2: 1,702,965-1,703,476 , GRCh37.p13 chr2: 1,706,737-1,707,248 PXDN
    nsv5877990copy number variation1nstd209human GRCh38 chr2: 1,703,023-1,703,946 , GRCh37.p13 chr2: 1,706,795-1,707,718 PXDN
    nsv5877710copy number variation1nstd209human GRCh38 chr2: 1,718,229-1,718,319 , GRCh37.p13 chr2: 1,722,001-1,722,091 PXDN
    nsv5875080copy number variation1nstd209human GRCh38 chr2: 1,637,522-1,637,595 , GRCh37.p13 chr2: 1,641,294-1,641,367 PXDN
    nsv5873947copy number variation1nstd209human GRCh38 chr2: 1,704,586-1,704,648 , GRCh37.p13 chr2: 1,708,358-1,708,420 PXDN
    nsv5873522copy number variation1nstd209human GRCh38 chr2: 1,639,031-1,639,082 , GRCh37.p13 chr2: 1,642,803-1,642,854 PXDN
    nsv5873212copy number variation1nstd209human GRCh38 chr2: 1,695,957-1,696,031 , GRCh37.p13 chr2: 1,699,729-1,699,803 PXDN
    nsv5870893copy number variation1nstd209human GRCh38 chr2: 1,703,110-1,704,139 , GRCh37.p13 chr2: 1,706,882-1,707,911 PXDN
    nsv5870200copy number variation1nstd209human GRCh38 chr2: 1,710,478-1,710,622 , GRCh37.p13 chr2: 1,714,250-1,714,394 PXDN
    nsv5869035copy number variation1nstd209human GRCh38 chr2: 1,719,915-1,720,143 , GRCh37.p13 chr2: 1,723,687-1,723,915 PXDN
    nsv5868739copy number variation1nstd209human GRCh38 chr2: 1,719,915-1,720,281 , GRCh37.p13 chr2: 1,723,687-1,724,053 PXDN
    nsv5868346copy number variation1nstd209human GRCh38 chr2: 1,703,005-1,704,269 , GRCh37.p13 chr2: 1,706,777-1,708,041 PXDN
    nsv5831940copy number variation1nstd209human GRCh38 chr2: 1,722,517-1,724,888 , GRCh37.p13 chr2: 1,726,289-1,728,660 PXDN
    nsv5624379insertion2nstd207human GRCh38 chr2: 1,710,791-1,710,791 , GRCh37.p13 chr2: 1,714,563-1,714,563 PXDN
    nsv5623688insertion1nstd207human GRCh38 chr2: 1,679,630-1,679,630 , GRCh37.p13 chr2: 1,683,402-1,683,402 PXDN
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