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Items: 1 to 20 of 226

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914830copy number variation1nstd209human GRCh38 chr8: 127,737,925-127,746,763 , GRCh37.p13 chr8: 128,750,171-128,759,009 MYC
    nsv5866544copy number variation1nstd209human GRCh38 chr8: 127,742,416-127,746,549 , GRCh37.p13 chr8: 128,754,662-128,758,795 MYC
    nsv5866318copy number variation1nstd209human GRCh38 chr8: 127,736,440-127,743,315 , GRCh37.p13 chr8: 128,748,686-128,755,561 MYC
    nsv5850629copy number variation1nstd209human GRCh38 chr8: 127,741,266-127,748,470 , GRCh37.p13 chr8: 128,753,512-128,760,716 MYC
    nsv5486226copy number variation1nstd206human GRCh38 chr8: 127,728,840-127,733,884 , GRCh37.p13 chr8: 128,741,086-128,746,130 CASC11, MYC
    nsv5477396copy number variation1nstd206human GRCh38 chr8: 127,737,925-127,746,764 , GRCh37.p13 chr8: 128,750,171-128,759,010 MYC
    nsv5379428translocation1nstd200human GRCh38 chr8: 127,746,764-127,746,764 , GRCh38 chr8: 127,737,925-127,737,925 , GRCh37.p13 chr8: 128,750,171-128,750,171 , GRCh37.p13 chr8: 128,759,010-128,759,010 MYC
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4680559copy number variation1nstd189human GRCh37.p13 chr8: 128,728,172-129,057,299 , GRCh38.p12 chr8: 127,715,926-128,045,053 MYC, PVT1, 7 more genes
    nsv4679605copy number variation1nstd189human GRCh37.p13 chr8: 128,664,766-128,863,886 , GRCh38.p12 chr8: 127,652,521-127,851,640 MYC, PVT1, 3 more genes
    nsv4679526copy number variation1nstd189human GRCh37.p13 chr8: 128,654,350-128,920,375 , GRCh38.p12 chr8: 127,642,105-127,908,129 MYC, PVT1, 3 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
    nsv4674996copy number variation1nstd102humanPathogenic GRCh37 chr8: 126,892,814-143,750,028 , GRCh38.p12 chr8: 125,880,570-142,668,610 POU5F1B, DNAJC8P3, 158 more genes
    nsv4578636copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 128,750,494-128,753,204 , GRCh38.p12 chr8: 127,738,248-127,740,958 MYC
    nsv4457220copy number variation1nstd102humanPathogenic GRCh37 chr8: 123,074,293-131,113,892 , GRCh38.p12 chr8: 122,062,054-130,101,646 ZHX1-C8orf76, SMILR, 117 more genes
    nsv4456997copy number variation1nstd102humanPathogenic GRCh37 chr8: 125,496,223-146,295,771 , GRCh38.p12 chr8: 124,483,982-145,070,385 LOC107986906, GPIHBP1, 317 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
    nsv4456783copy number variation1nstd102humanPathogenic GRCh37 chr8: 122,193,546-146,295,771 , GRCh38.p12 chr8: 121,181,306-145,070,385 HAS2, ZNF696, 369 more genes
    nsv4455511copy number variation1nstd102humanPathogenic GRCh37 chr8: 124,120,772-135,265,846 , GRCh38.p12 chr8: 123,108,532-134,253,603 MTSS1, PCAT2, 148 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
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