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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5934535copy number variation1nstd209human GRCh38 chr12: 120,296,963-120,300,022 , GRCh37.p13 chr12: 120,734,766-120,737,825 SIRT4
    nsv5863615copy number variation1nstd209human GRCh38 chr12: 120,297,582-120,298,781 , GRCh37.p13 chr12: 120,735,385-120,736,584 SIRT4
    nsv5707937mobile element insertion1nstd211human GRCh38 chr12: 120,297,347-120,297,347 , GRCh37.p13 chr12: 120,735,150-120,735,150 SIRT4
    nsv5594020copy number variation1nstd207human GRCh38 chr12: 120,306,296-120,307,678 , GRCh37.p13 chr12: 120,744,099-120,745,481 SIRT4
    nsv5503609copy number variation1nstd206human GRCh38 chr12: 120,299,844-120,299,989 , GRCh37.p13 chr12: 120,737,647-120,737,792 SIRT4
    nsv5502894copy number variation1nstd206human GRCh38 chr12: 120,306,313-120,307,679 , GRCh37.p13 chr12: 120,744,116-120,745,482 SIRT4
    nsv5500703copy number variation1nstd206human GRCh38 chr12: 120,313,560-120,314,817 , GRCh37.p13 chr12: 120,751,363-120,752,620 SIRT4, RNU6-1088P
    nsv5497083copy number variation1nstd206human GRCh38 chr12: 120,290,634-120,290,690 , GRCh37.p13 chr12: 120,728,437-120,728,493 RNU4-2, SIRT4
    nsv5495808copy number variation1nstd206human GRCh38 chr12: 120,308,139-120,308,484 , GRCh37.p13 chr12: 120,745,942-120,746,287 SIRT4
    nsv5494189copy number variation1nstd206human GRCh38 chr12: 120,307,864-120,311,306 , GRCh37.p13 chr12: 120,745,667-120,749,109 SIRT4, RNU6-1088P
    nsv5493978copy number variation1nstd206human GRCh38 chr12: 120,312,031-120,313,286 , GRCh37.p13 chr12: 120,749,834-120,751,089 RNU6-1088P, SIRT4
    nsv5332668translocation1nstd200human GRCh37 chr12: 120,745,972-120,745,972 , GRCh37 chr12: 120,746,242-120,746,242 , GRCh38.p12 chr12: 120,308,439-120,308,439 , GRCh38.p12 chr12: 120,308,169-120,308,169 SIRT4
    nsv5268819copy number variation1nstd204human GRCh38.p13 chr12: 120,302,001-120,317,500 , GRCh37.p13 chr12: 120,739,804-120,755,303 RNU6-1088P, SIRT4
    nsv5137952mobile element insertion1nstd203human GRCh38 chr12: 120,298,908-120,298,945 , GRCh37.p13 chr12: 120,736,711-120,736,748 SIRT4
    nsv5130659mobile element insertion1nstd203human GRCh38 chr12: 120,298,928-120,298,945 , GRCh37.p13 chr12: 120,736,731-120,736,748 SIRT4
    nsv4995969copy number variation1nstd200human GRCh38 chr12: 120,310,898-120,314,095 , GRCh37.p13 chr12: 120,748,701-120,751,898 RNU6-1088P, SIRT4
    nsv4995968copy number variation1nstd200human GRCh38 chr12: 120,307,394-120,309,060 , GRCh37.p13 chr12: 120,745,197-120,746,863 SIRT4
    nsv4995967copy number variation1nstd200human GRCh38 chr12: 120,306,326-120,307,660 , GRCh37.p13 chr12: 120,744,129-120,745,463 SIRT4
    nsv4995966copy number variation1nstd200human GRCh38 chr12: 120,299,844-120,299,989 , GRCh37.p13 chr12: 120,737,647-120,737,792 SIRT4
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