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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5724376mobile element insertion1nstd211human GRCh38 chr8: 134,860,929-134,860,929 , GRCh37.p13 chr8: 135,873,172-135,873,172 LOC101927845
    nsv5639895insertion1nstd207human GRCh38 chr8: 134,867,667-134,867,667 , GRCh37.p13 chr8: 135,879,910-135,879,910 LOC101927845
    nsv5562459mobile element insertion1nstd206human GRCh38 chr8: 134,860,929-134,860,980 , GRCh37.p13 chr8: 135,873,172-135,873,223 LOC101927845
    nsv5479550copy number variation1nstd206human GRCh38 chr8: 134,867,667-134,867,784 , GRCh37.p13 chr8: 135,879,910-135,880,027 LOC101927845
    nsv5387979copy number variation1nstd186human GRCh37 chr8: 135,879,910-135,880,027 , GRCh38.p12 chr8: 134,867,667-134,867,784 LOC101927845
    nsv5302838copy number variation1nstd204human GRCh38.p13 chr8: 134,867,658-134,867,792 , GRCh37.p13 chr8: 135,879,901-135,880,035 LOC101927845
    nsv5182778mobile element insertion1nstd203human GRCh38 chr8: 134,860,924-134,860,924 , GRCh37.p13 chr8: 135,873,167-135,873,167 LOC101927845
    nsv5116603mobile element insertion1nstd203human GRCh38 chr8: 134,860,648-134,860,658 , GRCh37.p13 chr8: 135,872,891-135,872,901 LOC101927845
    nsv5101894mobile element insertion1nstd203human GRCh38 chr8: 134,873,006-134,873,023 , GRCh37.p13 chr8: 135,885,249-135,885,266 LOC101927845
    nsv4962320copy number variation1nstd200human GRCh38 chr8: 134,865,453-134,870,971 , GRCh37.p13 chr8: 135,877,696-135,883,214 LOC101927845
    nsv4829321copy number variation1nstd200human GRCh37 chr8: 135,879,910-135,880,027 , GRCh38.p12 chr8: 134,867,667-134,867,784 LOC101927845
    nsv4755750insertion1nstd199human GRCh37 chr8: 135,879,959-135,879,959 , GRCh38.p12 chr8: 134,867,716-134,867,716 LOC101927845
    nsv4675664copy number variation1nstd102humanPathogenic GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385 LOC105375789, LINC02990, 270 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
    nsv4564667mobile element insertion1nstd166human GRCh37.p13 chr8: 135,873,156-135,873,156 , GRCh38.p12 chr8: 134,860,913-134,860,913 LOC101927845
    nsv4488235mobile element insertion1nstd166human GRCh37.p13 chr8: 135,872,891-135,872,891 , GRCh38.p12 chr8: 134,860,648-134,860,648 LOC101927845
    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
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