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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
    nsv7077335inversion1nstd229human GRCh38 chr8: 7,200,050-8,108,713 , GRCh37.p13 chr8: 7,057,572-7,966,235 OR7E96P, FAM90A8, 70 more genes
    nsv7074950inversion1nstd229human GRCh38 chr8: 7,147,097-8,343,791 , GRCh37.p13 chr8: 7,004,619-8,201,307 FAM90A10, ALG1L13P, 78 more genes
    nsv7071705inversion1nstd229human GRCh38 chr8: 7,041,770-8,576,733 , GRCh37.p13 chr8: 6,899,292-8,434,243 FAM90A7, SNRPCP15, 86 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
    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
    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
    nsv6636325copy number variation1nstd102humanUncertain significance GRCh37 chr8: 6,284,373-9,047,178 , GRCh38.p12 chr8: 6,426,852-9,189,668 DEFB105B, LOC105379216, 127 more genes
    nsv6634376copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-11,281,408 , GRCh38.p12 chr8: 208,048-11,423,899 DLGAP2-AS1, MIR124-1HG, 228 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6557746inversion1nstd223human GRCh38 chr8: 7,081,263-11,923,342 , GRCh37.p13 chr8: 6,938,785-11,780,851 BLK, LOC100420404, 157 more genes
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 LOC101928016, RPL23AP54, 568 more genes
    nsv6315342copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-10,348,413 , GRCh38.p12 chr8|NW_018654717.1: 1-5,513,617 , GRCh38.p12 chr8: 208,048-10,490,903 MIR1322, MIR548I3, 269 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6305614copy number variation1nstd186human GRCh37 chr8: 7,373,522-7,451,522 , GRCh38.p12 chr8: 7,516,000-7,594,000 , GRCh38.p12 chr8|NW_018654717.1: 655,251-703,356 , GRCh38.p12 chr8|NT_187570.1: 199,103-277,103 LOC105377800, FAM90A9, 15 more genes
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