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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7069370inversion1nstd229human GRCh38 chr8: 74,779,865-81,220,765 , GRCh37.p13 chr8: 75,692,100-82,133,000 THAP12P7, LOC105375905, 69 more genes
    nsv6853215copy number variation1nstd229human GRCh38 chr8: 75,371,044-80,542,313 , GRCh37.p13 chr8: 76,283,279-81,454,548 PKIA, LINC02605, 50 more genes
    nsv6849892copy number variation1nstd229human GRCh38 chr8: 79,827,702-79,847,485 , GRCh37.p13 chr8: 80,739,937-80,759,720 LOC101927040
    nsv6847993copy number variation1nstd229human GRCh38 chr8: 79,775,011-79,793,453 , GRCh37.p13 chr8: 80,687,246-80,705,688 LINC01607, LOC101927040
    nsv6843666copy number variation1nstd229human GRCh38 chr8: 79,870,601-79,877,400 , GRCh37.p13 chr8: 80,782,836-80,789,635 LOC101927040
    nsv6843261copy number variation1nstd229human GRCh38 chr8: 79,811,535-79,811,741 , GRCh37.p13 chr8: 80,723,770-80,723,976 LOC101927040
    nsv6843005copy number variation1nstd229human GRCh38 chr8: 77,380,887-79,895,467 , GRCh37.p13 chr8: 78,293,123-80,807,702 THAP12P7, LOC105375911, 23 more genes
    nsv6840818copy number variation1nstd229human GRCh38 chr8: 79,828,565-79,829,171 , GRCh37.p13 chr8: 80,740,800-80,741,406 LOC101927040
    nsv6636819copy number variation1nstd102humanUncertain significance GRCh37 chr8: 79,876,744-83,112,711 , GRCh38.p12 chr8: 78,964,509-82,200,476 SLC25A51P3, PMP2, 59 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6575523inversion1nstd223human GRCh38 chr8: 72,881,788-80,095,071 , GRCh37.p13 chr8: 73,794,023-81,007,306 ZFHX4-AS1, LINC01111, 82 more genes
    nsv6568252inversion1nstd223human GRCh38 chr8: 79,806,953-79,807,510 , GRCh37.p13 chr8: 80,719,188-80,719,745 LOC101927040
    nsv6435571copy number variation1nstd223human GRCh38 chr8: 79,781,501-79,785,900 , GRCh37.p13 chr8: 80,693,736-80,698,135 LINC01607, LOC101927040
    nsv6430301copy number variation1nstd223human GRCh38 chr8: 79,841,934-79,845,262 , GRCh37.p13 chr8: 80,754,169-80,757,497 LOC101927040
    nsv6419276copy number variation1nstd223human GRCh38 chr8: 79,758,601-79,792,500 , GRCh37.p13 chr8: 80,670,836-80,704,735 LOC101927040, HEY1, 1 more genes
    nsv6315163copy number variation1nstd102humanPathogenic GRCh37 chr8: 75,904,944-87,097,083 , GRCh38.p12 chr8: 74,992,709-86,084,854 ZNF704, RN7SL107P, 137 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6313579copy number variation1nstd102humanPathogenic GRCh37 chr8: 77,906,471-88,917,707 , GRCh38.p12 chr8: 76,994,235-87,905,479 LOC105375915, LOC105375918, 143 more genes
    nsv6246205mobile element insertion1nstd215human GRCh38 chr8: 79,852,656-79,852,656 , GRCh37.p13 chr8: 80,764,891-80,764,891 LOC101927040
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