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Items: 1 to 20 of 436

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958800insertion1nstd209human GRCh38 chr3: 47,431,267-47,431,267 , GRCh37.p13 chr3: 47,472,757-47,472,757 SCAP
    nsv5949937insertion1nstd209human GRCh38 chr3: 47,473,080-47,473,080 , GRCh37.p13 chr3: 47,514,570-47,514,570 SCAP
    nsv5903215copy number variation1nstd209human GRCh38 chr3: 47,430,153-47,533,200 , GRCh37.p13 chr3: 47,471,643-47,574,690 BOLA2P2, LOC105377073, 3 more genes
    nsv5891966copy number variation1nstd209human GRCh38 chr3: 47,449,177-47,451,949 , GRCh37.p13 chr3: 47,490,667-47,493,439 SCAP
    nsv5888582copy number variation1nstd209human GRCh38 chr3: 46,802,705-48,210,414 , GRCh37.p13 chr3: 46,844,195-48,251,904 SNORD13P3, LOC105377074, 34 more genes
    nsv5836580copy number variation2nstd209human GRCh38 chr3: 47,464,357-47,466,126 , GRCh37.p13 chr3: 47,505,847-47,507,616 SCAP
    nsv5836335copy number variation2nstd209human GRCh38 chr3: 47,455,963-47,477,359 , GRCh37.p13 chr3: 47,497,453-47,518,849 LOC105377073, SCAP
    nsv5836334copy number variation1nstd209human GRCh38 chr3: 47,449,169-47,451,968 , GRCh37.p13 chr3: 47,490,659-47,493,458 SCAP
    nsv5836333copy number variation2nstd209human GRCh38 chr3: 47,442,287-47,449,543 , GRCh37.p13 chr3: 47,483,777-47,491,033 SCAP
    nsv5836301copy number variation2nstd209human GRCh38 chr3: 47,426,653-47,444,618 , GRCh37.p13 chr3: 47,468,143-47,486,108 SCAP
    nsv5836027copy number variation2nstd209human GRCh38 chr3: 47,470,602-47,473,949 , GRCh37.p13 chr3: 47,512,092-47,515,439 SCAP
    nsv5836025copy number variation2nstd209human GRCh38 chr3: 47,431,953-47,433,454 , GRCh37.p13 chr3: 47,473,443-47,474,944 SCAP
    nsv5836024copy number variation2nstd209human GRCh38 chr3: 47,418,317-47,420,092 , GRCh37.p13 chr3: 47,459,807-47,461,582 SCAP
    nsv5615265insertion1nstd207human GRCh38 chr3: 47,431,267-47,431,267 , GRCh37.p13 chr3: 47,472,757-47,472,757 SCAP
    nsv5610673insertion1nstd207human GRCh38 chr3: 47,416,784-47,416,784 , GRCh37.p13 chr3: 47,458,274-47,458,274 SCAP
    nsv5610650insertion1nstd207human GRCh38 chr3: 47,417,894-47,417,894 , GRCh37.p13 chr3: 47,459,384-47,459,384 SCAP
    nsv5569026copy number variation1nstd207human GRCh38 chr3: 47,449,177-47,451,949 , GRCh37.p13 chr3: 47,490,667-47,493,439 SCAP
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5544749insertion1nstd206human GRCh38 chr3: 47,431,267-47,431,267 , GRCh37.p13 chr3: 47,472,757-47,472,757 SCAP
    nsv5539869insertion1nstd206human GRCh38 chr3: 47,435,526-47,435,577 , GRCh37.p13 chr3: 47,477,016-47,477,067 SCAP
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