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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
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7142185insertion1nstd232human GRCh37.p13 chr8: 23,404,071-23,404,071 , GRCh38.p12 chr8: 23,546,558-23,546,558 SLC25A37
    nsv7098901copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 21,925,038-26,372,195 , GRCh38.p12 chr8: 22,067,527-26,514,679 BMP1, POLR3D, 95 more genes
    nsv7073429inversion1nstd229human GRCh38 chr8: 22,689,880-24,095,801 , GRCh37.p13 chr8: 22,547,393-23,953,314 TNFRSF10B, RNU1-148P, 34 more genes
    nsv6855871copy number variation1nstd229human GRCh38 chr8: 23,452,001-23,587,300 , GRCh37.p13 chr8: 23,309,514-23,444,813 ENTPD4, SLC25A37, 2 more genes
    nsv6854214copy number variation1nstd229human GRCh38 chr8: 23,529,212-23,566,105 , GRCh37.p13 chr8: 23,386,725-23,423,618 SLC25A37
    nsv6849816copy number variation1nstd229human GRCh38 chr8: 23,572,216-23,572,249 , GRCh37.p13 chr8: 23,429,729-23,429,762 SLC25A37
    nsv6848647copy number variation1nstd229human GRCh38 chr8: 23,522,027-23,527,239 , GRCh37.p13 chr8: 23,379,540-23,384,752 SLC25A37
    nsv6847925copy number variation1nstd229human GRCh38 chr8: 23,531,044-23,536,515 , GRCh37.p13 chr8: 23,388,557-23,394,028 SLC25A37
    nsv6845136copy number variation1nstd229human GRCh38 chr8: 23,549,710-23,550,346 , GRCh37.p13 chr8: 23,407,223-23,407,859 SLC25A37
    nsv6844201copy number variation1nstd229human GRCh38 chr8: 23,546,009-23,549,883 , GRCh37.p13 chr8: 23,403,522-23,407,396 SLC25A37
    nsv6842954copy number variation1nstd229human GRCh38 chr8: 22,958,501-23,751,500 , GRCh37.p13 chr8: 22,816,014-23,609,013 TNFRSF10B, RNU4-71P, 23 more genes
    nsv6842596copy number variation1nstd229human GRCh38 chr8: 23,526,301-23,527,200 , GRCh37.p13 chr8: 23,383,814-23,384,713 SLC25A37
    nsv6839950copy number variation1nstd229human GRCh38 chr8: 23,568,378-23,571,332 , GRCh37.p13 chr8: 23,425,891-23,428,845 SLC25A37
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6565031inversion1nstd223human GRCh38 chr8: 22,900,235-30,247,902 , GRCh37.p13 chr8: 22,757,748-30,105,418 LOC105379349, MIR6876, 140 more genes
    nsv6429716copy number variation1nstd223human GRCh38 chr8: 22,969,514-24,288,515 , GRCh37.p13 chr8: 22,827,027-24,146,028 NKX3-1, LOC107984124, 27 more genes
    nsv6429459copy number variation1nstd223human GRCh38 chr8: 23,296,973-23,543,937 , GRCh37.p13 chr8: 23,154,486-23,401,450 LOXL2, SLC25A37, 4 more genes
    nsv6426872copy number variation1nstd223human GRCh38 chr8: 23,545,984-23,549,880 , GRCh37.p13 chr8: 23,403,497-23,407,393 SLC25A37
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