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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
    nsv7148131copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120 XKR6, FAM90A11, 224 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
    nsv7074774inversion1nstd229human GRCh38 chr8: 7,765,163-10,984,073 , GRCh37.p13 chr8: 7,622,685-10,841,583 PRSS52P, PPP1R3B-DT, 81 more genes
    nsv7071894inversion1nstd229human GRCh38 chr8: 8,228,418-10,333,532 , GRCh37.p13 chr8: 8,085,940-10,191,042 RN7SL178P, LOC107986914, 33 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
    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
    nsv6857430copy number variation1nstd229human GRCh38 chr8: 8,565,014-8,887,036 , GRCh37.p13 chr8: 8,422,524-8,744,546 LOC105379225, MFHAS1, 3 more genes
    nsv6856656copy number variation1nstd229human GRCh38 chr8: 8,801,191-8,803,949 , GRCh37.p13 chr8: 8,658,701-8,661,459 MFHAS1
    nsv6854187copy number variation1nstd229human GRCh38 chr8: 8,884,062-8,884,083 , GRCh37.p13 chr8: 8,741,572-8,741,593 MFHAS1
    nsv6854113copy number variation1nstd229human GRCh38 chr8: 8,818,156-8,825,927 , GRCh37.p13 chr8: 8,675,666-8,683,437 MFHAS1
    nsv6854070copy number variation1nstd229human GRCh38 chr8: 8,837,801-8,868,200 , GRCh37.p13 chr8: 8,695,311-8,725,710 MFHAS1
    nsv6853472copy number variation1nstd229human GRCh38 chr8: 8,846,072-9,367,802 , GRCh37.p13 chr8: 8,703,582-9,225,312 LOC101929128, LOC105379228, 16 more genes
    nsv6852439copy number variation1nstd229human GRCh38 chr8: 8,818,733-8,844,118 , GRCh37.p13 chr8: 8,676,243-8,701,628 MFHAS1
    nsv6851957copy number variation1nstd229human GRCh38 chr8: 8,774,594-8,784,300 , GRCh37.p13 chr8: 8,632,104-8,641,810 MFHAS1
    nsv6851428copy number variation1nstd229human GRCh38 chr8: 8,804,583-8,829,730 , GRCh37.p13 chr8: 8,662,093-8,687,240 MFHAS1
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