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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5974801inversion1nstd209human GRCh38 chr10: 116,446,135-119,236,441 , GRCh37.p13 chr10: 118,205,647-120,995,953 EMX2, PRLHR, 48 more genes
    nsv5711508mobile element insertion1nstd211human GRCh38 chr10: 117,528,859-117,528,859 , GRCh37.p13 chr10: 119,288,370-119,288,370 EMX2OS
    nsv5672603copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 119,302,758-124,813,305 , GRCh38.p12 chr10: 117,543,247-123,053,789 ACADSB, DMBT1, 84 more genes
    nsv5638712insertion1nstd207human GRCh38 chr10: 117,485,540-117,485,540 , GRCh37.p13 chr10: 119,245,051-119,245,051 EMX2OS
    nsv5551798insertion1nstd206human GRCh38 chr10: 117,485,560-117,485,591 , GRCh37.p13 chr10: 119,245,071-119,245,102 EMX2OS
    nsv5510453copy number variation1nstd206human GRCh38 chr10: 117,536,614-117,536,737 , GRCh37.p13 chr10: 119,296,125-119,296,248 EMX2OS
    nsv5400634mobile element insertion1nstd206human GRCh38 chr10: 117,528,859-117,528,910 , GRCh37.p13 chr10: 119,288,370-119,288,421 EMX2OS
    nsv5301626copy number variation1nstd204human GRCh38.p13 chr10: 117,479,647-117,491,595 , GRCh37.p13 chr10: 119,239,158-119,251,106 EMX2OS
    nsv5256254copy number variation1nstd204human GRCh38.p13 chr10: 117,479,699-117,492,544 , GRCh37.p13 chr10: 119,239,210-119,252,055 EMX2OS
    nsv5185512mobile element insertion1nstd203human GRCh38 chr10: 117,509,644-117,509,663 , GRCh37.p13 chr10: 119,269,155-119,269,174 EMX2OS
    nsv5139598mobile element insertion1nstd203human GRCh38 chr10: 117,485,544-117,485,560 , GRCh37.p13 chr10: 119,245,055-119,245,071 EMX2OS
    nsv5121138mobile element insertion1nstd203human GRCh38 chr10: 117,485,540-117,485,560 , GRCh37.p13 chr10: 119,245,051-119,245,071 EMX2OS
    nsv4977132copy number variation1nstd200human GRCh38 chr10: 117,502,907-117,503,584 , GRCh37.p13 chr10: 119,262,418-119,263,095 EMX2OS
    nsv4977131copy number variation1nstd200human GRCh38 chr10: 117,479,650-117,491,593 , GRCh37.p13 chr10: 119,239,161-119,251,104 EMX2OS
    nsv4974087copy number variation1nstd200human GRCh38 chr10: 117,535,309-117,887,959 , GRCh37.p13 chr10: 119,294,820-119,647,470 LINC02674, LOC107984274, 2 more genes
    nsv4849274copy number variation1nstd200human GRCh37 chr10: 119,262,418-119,263,095 , GRCh38.p12 chr10: 117,502,907-117,503,584 EMX2OS
    nsv4848160copy number variation1nstd200human GRCh37 chr10: 119,239,161-119,251,104 , GRCh38.p12 chr10: 117,479,650-117,491,593 EMX2OS
    nsv4838613copy number variation1nstd200human GRCh37 chr10: 119,296,125-119,296,248 , GRCh38.p12 chr10: 117,536,614-117,536,737 EMX2OS
    nsv4541388insertion1nstd166human GRCh37.p13 chr10: 119,245,051-119,245,051 , GRCh38.p12 chr10: 117,485,540-117,485,540 EMX2OS
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