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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148110copy number variation1nstd102humanPathogenic GRCh37 chr8: 7,080,281-12,045,269 , GRCh38.p12 chr8: 7,222,759-12,187,760 DEFB106A, LOC101927997, 176 more genes
    nsv7070191inversion1nstd229human GRCh38 chr8: 11,431,142-11,714,759 , GRCh37.p13 chr8: 11,288,651-11,572,268 BLK, GATA4, 6 more genes
    nsv7069609inversion1nstd229human GRCh38 chr8: 7,102,414-12,683,056 , GRCh37.p13 chr8: 6,959,936-12,540,565 FAM90A20, LOC107986910, 201 more genes
    nsv7067997inversion1nstd229human GRCh38 chr8: 8,181,479-12,388,066 , GRCh37.p13 chr8: 8,039,001-12,245,575 TNKS, ZNF705D, 113 more genes
    nsv7065354inversion1nstd229human GRCh38 chr8: 9,129,798-15,405,439 , GRCh37.p13 chr8: 8,987,308-15,262,948 FAM167A, LOC729732, 132 more genes
    nsv7062538inversion1nstd229human GRCh38 chr8: 7,137,678-12,551,118 , GRCh37.p13 chr8: 6,995,200-12,408,627 MIR124-1, MFHAS1, 197 more genes
    nsv7060774inversion1nstd229human GRCh38 chr8: 7,366,932-11,853,836 , GRCh37.p13 chr8: 7,224,454-11,711,345 DEFB104B, SNORA99, 135 more genes
    nsv7059146inversion1nstd229human GRCh38 chr8: 7,352,588-12,547,775 , GRCh37.p13 chr8: 7,210,110-12,405,284 LOC107986910, HSPD1P2, 179 more genes
    nsv7058956inversion1nstd229human GRCh38 chr8: 8,224,000-12,734,745 , GRCh37.p13 chr8: 8,081,522-12,592,254 MIR3926-1, FAM90A25P, 129 more genes
    nsv6854641copy number variation1nstd229human GRCh38 chr8: 11,571,543-11,591,628 , GRCh37.p13 chr8: 11,429,052-11,449,137 LINC00208
    nsv6853760copy number variation1nstd229human GRCh38 chr8: 11,531,738-11,611,042 , GRCh37.p13 chr8: 11,389,247-11,468,551 LINC00208, BLK, 1 more genes
    nsv6852641copy number variation1nstd229human GRCh38 chr8: 11,575,180-11,577,540 , GRCh37.p13 chr8: 11,432,689-11,435,049 LINC00208
    nsv6850256copy number variation1nstd229human GRCh38 chr8: 11,539,713-11,633,714 , GRCh37.p13 chr8: 11,397,222-11,491,223 LINC00208, LOC105379242, 2 more genes
    nsv6848257copy number variation1nstd229human GRCh38 chr8: 11,533,196-11,722,248 , GRCh37.p13 chr8: 11,390,705-11,579,757 SNORA99, LINC00208, 4 more genes
    nsv6842641copy number variation1nstd229human GRCh38 chr8: 11,579,418-11,582,379 , GRCh37.p13 chr8: 11,436,927-11,439,888 LINC00208
    nsv6637100copy number variation1nstd102humanUncertain significance GRCh37 chr8: 11,196,295-11,521,748 , GRCh38.p12 chr8: 11,338,786-11,664,239 , GRCh38.p12 chr8|NW_018654717.1: 1,683,832-2,008,059 RNU6-1084P, TDH, 8 more genes
    nsv6636968copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-18,936,715 , GRCh38.p12 chr8: 208,049-19,079,205 ZNF705B, NATP, 357 more genes
    nsv6636940copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-10,965,627 , GRCh38.p12 chr8|NW_018654717.1: 1-5,513,617 , GRCh38.p12 chr8: 208,049-11,108,117 HSPD1P3, LOC401442, 270 more genes
    nsv6636617copy number variation1nstd102humanPathogenic GRCh37 chr8: 8,093,066-12,548,732 , GRCh38.p12 chr8: 8,235,544-12,691,223 , GRCh38.p12 chr8|NW_018654717.1: 996,517-5,112,321 DEFB131D, RNU6-682P, 128 more genes
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