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Items: 1 to 20 of 416

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966891insertion1nstd209human GRCh38 chr8: 22,423,786-22,423,786 , GRCh37.p13 chr8: 22,281,299-22,281,299 SLC39A14
    nsv5920605copy number variation1nstd209human GRCh38 chr8: 22,403,014-22,403,316 , GRCh37.p13 chr8: 22,260,527-22,260,829 SLC39A14
    nsv5703016mobile element insertion2nstd211human GRCh38 chr8: 22,375,228-22,375,228 , GRCh37.p13 chr8: 22,232,741-22,232,741 SLC39A14
    nsv5571607copy number variation1nstd207human GRCh38 chr8: 22,396,412-22,396,538 , GRCh37.p13 chr8: 22,253,925-22,254,051 SLC39A14
    nsv5486987copy number variation1nstd206human GRCh38 chr8: 22,371,412-22,371,485 , GRCh37.p13 chr8: 22,228,925-22,228,998 SLC39A14
    nsv5484601copy number variation1nstd206human GRCh38 chr8: 22,422,927-22,426,787 , GRCh37.p13 chr8: 22,280,440-22,284,300 SLC39A14
    nsv5480173copy number variation1nstd206human GRCh38 chr8: 22,404,078-22,404,153 , GRCh37.p13 chr8: 22,261,591-22,261,666 SLC39A14
    nsv5479844copy number variation1nstd206human GRCh38 chr8: 22,418,785-22,418,998 , GRCh37.p13 chr8: 22,276,298-22,276,511 SLC39A14
    nsv5406291mobile element insertion1nstd206human GRCh38 chr8: 22,375,228-22,375,261 , GRCh37.p13 chr8: 22,232,741-22,232,774 SLC39A14
    nsv5312207copy number variation1nstd204human GRCh37.p13 chr8: 22,284,769-22,370,475 , GRCh38.p13 chr8: 22,427,256-22,512,962 PPP3CC, SLC39A14, 2 more genes
    nsv5308315copy number variation1nstd204human GRCh38.p13 chr8: 22,371,406-22,371,490 , GRCh37.p13 chr8: 22,228,919-22,229,003 SLC39A14
    nsv5250621copy number variation1nstd204human GRCh38.p13 chr8: 22,427,201-22,443,688 , GRCh37.p13 chr8: 22,284,714-22,301,201 PPP3CC, SLC39A14, 1 more genes
    nsv5248629copy number variation1nstd204human GRCh38.p13 chr8: 22,427,201-22,513,000 , GRCh37.p13 chr8: 22,284,714-22,370,513 PPP3CC, RNU6-336P, 2 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4959652copy number variation1nstd200human GRCh38 chr8: 22,371,412-22,371,485 , GRCh37.p13 chr8: 22,228,925-22,228,998 SLC39A14
    nsv4954259copy number variation1nstd200human GRCh38 chr8: 22,430,773-22,450,175 , GRCh37.p13 chr8: 22,288,286-22,307,688 SLC39A14, PPP3CC, 1 more genes
    nsv4954257copy number variation1nstd200human GRCh38 chr8: 22,358,150-22,384,033 , GRCh37.p13 chr8: 22,215,663-22,241,546 SLC39A14
    nsv4954256copy number variation1nstd200human GRCh38 chr8: 22,351,525-22,520,784 , GRCh37.p13 chr8: 22,209,038-22,378,297 SLC39A14, PPP3CC, 4 more genes
    nsv4825681copy number variation1nstd200human GRCh37 chr8: 22,282,035-22,282,189 , GRCh38.p12 chr8: 22,424,522-22,424,676 SLC39A14
    nsv4821471copy number variation1nstd200human GRCh37 chr8: 22,228,925-22,228,998 , GRCh38.p12 chr8: 22,371,412-22,371,485 SLC39A14
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