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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
    nsv7148128copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 10,501-6,614,959 , GRCh38.p12 chr8: 60,501-6,757,438 ANGPT2, CLN8, 67 more genes
    nsv7074214inversion1nstd229human GRCh38 chr8: 1,202,764-2,370,937 , GRCh37.p13 chr8: 1,152,764-1,965,389 LOC105377781, MYOM2, 21 more genes
    nsv7072453inversion1nstd229human GRCh38 chr8: 1,726,108-1,890,961 , GRCh37.p13 chr8: 1,674,274-1,839,127 ARHGEF10, MIR596, 6 more genes
    nsv7068644inversion1nstd229human GRCh38 chr8: 496,129-6,118,991 , GRCh37.p13 chr8: 446,129-5,976,513 LOC105377795, LOC100131395, 47 more genes
    nsv7062154inversion1nstd229human GRCh38 chr8: 1,744,685-2,489,179 , GRCh37.p13 chr8: 1,692,851-2,346,295 LOC105377782, KBTBD11, 15 more genes
    nsv7059889inversion1nstd229human GRCh38 chr8: 1,445,340-4,898,472 , GRCh37.p13 chr8: 1,393,506-4,755,994 LOC105377790, RNA5SP251, 27 more genes
    nsv7059725inversion1nstd229human GRCh38 chr8: 1,763,772-1,978,955 , GRCh37.p13 chr8: 1,711,938-1,927,121 KBTBD11, LOC105377779, 8 more genes
    nsv7059594inversion1nstd229human GRCh38 chr8: 441,112-6,103,891 , GRCh37.p13 chr8: 391,112-5,961,413 LOC286083, MIR3674, 48 more genes
    nsv6857566copy number variation1nstd229human GRCh38 chr8: 1,725,601-1,890,700 , GRCh37.p13 chr8: 1,673,767-1,838,866 CLN8-AS1, LOC100130321, 6 more genes
    nsv6855534copy number variation1nstd229human GRCh38 chr8: 1,731,753-1,820,606 , GRCh37.p13 chr8: 1,679,919-1,768,772 LOC105377778, MIR3674, 4 more genes
    nsv6853940copy number variation1nstd229human GRCh38 chr8: 1,754,486-1,760,161 , GRCh37.p13 chr8: 1,702,652-1,708,327 CLN8-AS1, CLN8, 1 more genes
    nsv6853623copy number variation1nstd229human GRCh38 chr8: 1,548,337-1,907,422 , GRCh37.p13 chr8: 1,496,503-1,855,588 MIR3674, LOC105377778, 8 more genes
    nsv6853105copy number variation1nstd229human GRCh38 chr8: 1,742,368-1,829,609 , GRCh37.p13 chr8: 1,690,534-1,777,775 LOC105377778, MIR3674, 5 more genes
    nsv6848952copy number variation1nstd229human GRCh38 chr8: 1,373,465-1,774,850 , GRCh37.p13 chr8: 1,321,631-1,723,016 LOC100130321, CLN8, 7 more genes
    nsv6844953copy number variation1nstd229human GRCh38 chr8: 1,730,746-1,834,063 , GRCh37.p13 chr8: 1,678,912-1,782,229 CLN8, LOC100130321, 6 more genes
    nsv6840028copy number variation1nstd229human GRCh38 chr8: 1,746,087-1,807,740 , GRCh37.p13 chr8: 1,694,253-1,755,906 CLN8-AS1, LOC105377778, 2 more genes
    nsv6826699copy number variation1nstd229human GRCh38 chr8: 320,397-3,564,517 , GRCh37.p13 chr8: 270,397-3,422,039 MIR596, LOC105377781, 33 more genes
    nsv6637154copy number variation1nstd102humanUncertain significance GRCh37 chr8: 1,446,994-1,881,289 , GRCh38.p12 chr8|NT_187680.1: 1-229,282 , GRCh38.p12 chr8: 1,498,828-1,933,123 DLGAP2, CLN8, 9 more genes
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