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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922878copy number variation1nstd209human GRCh38 chr8: 101,483,803-101,484,100 , GRCh37.p13 chr8: 102,496,031-102,496,328
    nsv5914773copy number variation1nstd209human GRCh38 chr8: 101,467,117-101,469,405 , GRCh37.p13 chr8: 102,479,345-102,481,633
    nsv5858848copy number variation1nstd209human GRCh38 chr8: 101,467,124-101,469,443 , GRCh37.p13 chr8: 102,479,352-102,481,671
    nsv5493078copy number variation1nstd206human GRCh38 chr8: 101,468,785-101,468,877 , GRCh37.p13 chr8: 102,481,013-102,481,105
    nsv5485256copy number variation1nstd206human GRCh38 chr8: 101,467,117-101,469,406 , GRCh37.p13 chr8: 102,479,345-102,481,634
    nsv5372066translocation1nstd200human GRCh38 chr8: 101,490,640-101,490,640 , GRCh38 chr8: 101,490,768-101,490,768 , GRCh37.p13 chr8: 102,502,868-102,502,868 , GRCh37.p13 chr8: 102,502,996-102,502,996 , GRHL2, 1 more genes
    nsv5372065translocation1nstd200human GRCh38 chr8: 101,467,117-101,467,117 , GRCh38 chr8: 101,469,406-101,469,406 , GRCh37.p13 chr8: 102,479,345-102,479,345 , GRCh37.p13 chr8: 102,481,634-102,481,634
    nsv5114097mobile element insertion1nstd203human GRCh38 chr8: 101,473,928-101,473,936 , GRCh37.p13 chr8: 102,486,156-102,486,164
    nsv5111618mobile element insertion1nstd203human GRCh38 chr8: 101,473,931-101,473,936 , GRCh37.p13 chr8: 102,486,159-102,486,164
    nsv5109646mobile element insertion1nstd203human GRCh38 chr8: 101,473,922-101,473,936 , GRCh37.p13 chr8: 102,486,150-102,486,164
    nsv5107980mobile element insertion1nstd203human GRCh38 chr8: 101,473,936-101,473,984 , GRCh37.p13 chr8: 102,486,164-102,486,212
    nsv5102094mobile element insertion1nstd203human GRCh38 chr8: 101,483,267-101,483,277 , GRCh37.p13 chr8: 102,495,495-102,495,505
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4965659copy number variation1nstd200human GRCh38 chr8: 101,456,362-101,486,798 , GRCh37.p13 chr8: 102,468,590-102,499,026
    nsv4965657copy number variation1nstd200human GRCh38 chr8: 101,445,347-101,487,017 , GRCh37.p13 chr8: 102,457,575-102,499,245
    nsv4829212copy number variation1nstd200human GRCh37 chr8: 102,468,590-102,499,026 , GRCh38.p12 chr8: 101,456,362-101,486,798
    nsv4829211copy number variation1nstd200human GRCh37 chr8: 102,457,575-102,499,245 , GRCh38.p12 chr8: 101,445,347-101,487,017
    nsv4822656copy number variation1nstd200human GRCh37 chr8: 102,479,345-102,481,634 , GRCh38.p12 chr8: 101,467,117-101,469,406
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
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