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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925029copy number variation1nstd209human GRCh38 chr8: 35,698,163-35,698,238 , GRCh37.p13 chr8: 35,555,681-35,555,756 UNC5D, LOC101929550
    nsv5491895copy number variation1nstd206human GRCh38 chr8: 35,698,166-35,698,239 , GRCh37.p13 chr8: 35,555,684-35,555,757 LOC101929550, UNC5D
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5110538mobile element insertion1nstd203human GRCh38 chr8: 35,703,092-35,703,100 , GRCh37.p13 chr8: 35,560,610-35,560,618 LOC101929550, UNC5D
    nsv4954341copy number variation1nstd200human GRCh38 chr8: 35,693,318-35,717,899 , GRCh37.p13 chr8: 35,550,836-35,575,417 UNC5D, LOC101929550
    nsv4954340copy number variation1nstd200human GRCh38 chr8: 35,689,539-35,689,715 , GRCh37.p13 chr8: 35,547,057-35,547,233 UNC5D, LOC101929550
    nsv4827365copy number variation1nstd200human GRCh37 chr8: 35,550,307-35,556,041 , GRCh38.p12 chr8: 35,692,789-35,698,523 UNC5D, LOC101929550
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4680683copy number variation1nstd189human GRCh37.p13 chr8: 35,047,789-36,164,231 , GRCh38.p12 chr8: 35,190,271-36,306,713 , UNC5D, 7 more genes
    nsv4651500copy number variation1nstd186human GRCh37 chr8: 35,568,203-35,568,620 , GRCh38.p12 chr8: 35,710,685-35,711,102 LOC101929550, UNC5D
    nsv4610920copy number variation1nstd183human GRCh37 chr8: 35,489,569-35,729,585 , GRCh38.p12 chr8: 35,632,051-35,872,067 LOC101929550, UNC5D
    nsv4527001copy number variation1nstd166human GRCh37.p13 chr8: 35,568,203-35,568,620 , GRCh38.p12 chr8: 35,710,685-35,711,102 UNC5D, LOC101929550
    nsv4494763mobile element insertion1nstd166human GRCh37.p13 chr8: 35,560,610-35,560,610 , GRCh38.p12 chr8: 35,703,092-35,703,092 UNC5D, LOC101929550
    nsv4457019copy number variation1nstd102humanUncertain significance GRCh37 chr8: 29,103,983-35,728,509 , GRCh38.p12 chr8: 29,246,466-35,870,991 TAGLN2P2, GSR, 87 more genes
    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
    nsv4407403copy number variation1nstd174human GRCh37 chr8: 35,568,225-35,568,773 , GRCh38.p12 chr8: 35,710,707-35,711,255 LOC101929550, UNC5D
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4348018copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,546,855-35,816,855 , GRCh38.p12 chr8: 12,689,346-35,959,337 NAT1, NAT2, 343 more genes
    nsv4323300inversion1nstd166human GRCh37.p13 chr8: 33,635,229-36,339,673 , GRCh38.p12 chr8: 33,777,711-36,482,155 , LSM12P1, 18 more genes
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