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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926477copy number variation1nstd209human GRCh38 chr8: 37,730,409-37,731,337 , GRCh37.p13 chr8: 37,587,927-37,588,855 LOC101929622
    nsv5907897copy number variation1nstd209human GRCh38 chr8: 37,719,760-37,719,813 , GRCh37.p13 chr8: 37,577,278-37,577,331 LOC101929622
    nsv5639446insertion2nstd207human GRCh38 chr8: 37,719,760-37,719,760 , GRCh37.p13 chr8: 37,577,278-37,577,278 LOC101929622
    nsv5540176insertion1nstd206human GRCh38 chr8: 37,719,710-37,719,752 , GRCh37.p13 chr8: 37,577,228-37,577,270 LOC101929622
    nsv5476954copy number variation1nstd206human GRCh38 chr8: 37,730,424-37,731,306 , GRCh37.p13 chr8: 37,587,942-37,588,824 LOC101929622
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4827413copy number variation1nstd200human GRCh37 chr8: 37,587,940-37,588,846 , GRCh38.p12 chr8: 37,730,422-37,731,328 LOC101929622
    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
    nsv4723618insertion1nstd186human GRCh37 chr8: 37,577,278-37,577,278 , GRCh38.p12 chr8: 37,719,760-37,719,760 LOC101929622
    nsv4703839copy number variation1nstd195human GRCh37 chr8: 37,323,851-37,784,501 , GRCh38.p12 chr8: 37,466,333-37,926,983 LOC101929622, LOC102723701, 14 more genes
    nsv4556458insertion1nstd166human GRCh37.p13 chr8: 37,577,278-37,577,278 , GRCh38.p12 chr8: 37,719,760-37,719,760 LOC101929622
    nsv4538685insertion1nstd166human GRCh37.p13 chr8: 37,577,270-37,577,270 , GRCh38.p12 chr8: 37,719,752-37,719,752 LOC101929622
    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
    nsv4456199copy number variation1nstd102humanUncertain significance GRCh37 chr8: 36,094,421-43,822,214 , GRCh38.p12 chr8: 36,236,903-43,967,071 AFG3L2P1, BRF2, 136 more genes
    nsv4436744copy number variation1nstd102humanUncertain significance GRCh37 chr8: 36,486,830-37,992,515 , GRCh38.p12 chr8: 36,629,312-38,134,997 LOC105379380, LOC728024, 29 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4166590copy number variation1nstd166human GRCh37.p13 chr8: 37,591,000-37,597,000 , GRCh38.p12 chr8: 37,733,482-37,739,482 LOC101929622, LOC102723701, 1 more genes
    nsv4154921copy number variation1nstd166human GRCh37.p13 chr8: 37,587,757-37,588,652 , GRCh38.p12 chr8: 37,730,239-37,731,134 LOC101929622
    nsv4152833copy number variation1nstd166human GRCh37.p13 chr8: 37,573,482-37,573,726 , GRCh38.p12 chr8: 37,715,964-37,716,208 LOC101929622
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