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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961225insertion1nstd209human GRCh38 chr8: 77,000,372-77,000,372 , GRCh37.p13 chr8: 77,912,608-77,912,608 PEX2
    nsv5919342copy number variation1nstd209human GRCh38 chr8: 72,905,491-79,590,734 , GRCh37.p13 chr8: 73,817,726-80,502,969 , GYG1P1, 73 more genes
    nsv5916690copy number variation1nstd209human GRCh38 chr8: 76,990,688-76,990,737 , GRCh37.p13 chr8: 77,902,924-77,902,973 PEX2
    nsv5542538insertion1nstd206human GRCh38 chr8: 77,000,382-77,000,422 , GRCh37.p13 chr8: 77,912,618-77,912,658 PEX2
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv5033690inversion1nstd200human GRCh38 chr8: 74,725,992-77,381,341 , GRCh37.p13 chr8: 75,638,227-78,293,577 CASC9, LOC107986952, 17 more genes
    nsv4965494copy number variation1nstd200human GRCh38 chr8: 76,731,294-77,168,383 , GRCh37.p13 chr8: 77,643,530-78,080,619 ZFHX4, PEX2, 2 more genes
    nsv4961039copy number variation1nstd200human GRCh38 chr8: 76,996,198-76,997,205 , GRCh37.p13 chr8: 77,908,434-77,909,441 PEX2
    nsv4876764inversion1nstd200human GRCh37 chr8: 75,638,227-78,293,577 , GRCh38.p12 chr8: 74,725,992-77,381,341 LINC01111, LOC102724858, 17 more genes
    nsv4822059copy number variation1nstd200human GRCh37 chr8: 77,908,434-77,909,441 , GRCh38.p12 chr8: 76,996,198-76,997,205 PEX2
    nsv4721980insertion1nstd186human GRCh37 chr8: 77,912,596-77,912,596 , GRCh38.p12 chr8: 77,000,360-77,000,360 PEX2
    nsv4599975copy number variation1nstd183human GRCh37 chr8: 77,912,887-77,932,985 , GRCh38.p12 chr8: 77,000,651-77,020,749 PEX2, HIGD1AP18
    nsv4552415insertion1nstd166human GRCh37.p13 chr8: 77,912,596-77,912,596 , GRCh38.p12 chr8: 77,000,360-77,000,360 PEX2
    nsv4492554mobile element insertion1nstd166human GRCh37.p13 chr8: 77,895,791-77,895,791 , GRCh38.p12 chr8: 76,983,555-76,983,555 PEX2
    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
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4332062inversion1nstd166human GRCh37.p13 chr8: 70,438,609-99,073,700 , GRCh38.p12 chr8: 69,526,374-98,061,472 , FTH1P11, 375 more genes
    nsv4318515inversion1nstd166human GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713 , ANXA13, 716 more genes
    nsv4169695copy number variation1nstd166human GRCh37.p13 chr8: 77,248,037-78,500,368 , GRCh38.p12 chr8: 76,335,802-77,588,132 LOC102724874, LINC01111, 8 more genes
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