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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
    nsv7098732copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,915,043-20,112,692 , GRCh38.p12 chr8: 18,057,534-20,255,181 LOC107986868, ASAH1-AS1, 31 more genes
    nsv7074820inversion1nstd229human GRCh38 chr8: 17,929,527-19,508,705 , GRCh37.p13 chr8: 17,787,036-19,366,216 PSD3, LOC442382, 20 more genes
    nsv7071559inversion1nstd229human GRCh38 chr8: 15,858,861-19,517,388 , GRCh37.p13 chr8: 15,716,370-19,374,899 MTMR7, ADAM24P, 45 more genes
    nsv7071155inversion1nstd229human GRCh38 chr8: 19,297,879-19,350,041 , GRCh37.p13 chr8: 19,155,390-19,207,552 SH2D4A, LOC105379306
    nsv6857761copy number variation1nstd229human GRCh38 chr8: 19,287,601-19,620,000 , GRCh37.p13 chr8: 19,145,112-19,477,511 LOC105379306, CSGALNACT1, 1 more genes
    nsv6857542copy number variation1nstd229human GRCh38 chr8: 18,998,582-19,578,893 , GRCh37.p13 chr8: 18,856,092-19,436,404 LOC105379306, LOC105379303, 7 more genes
    nsv6856083copy number variation1nstd229human GRCh38 chr8: 19,298,974-19,306,723 , GRCh37.p13 chr8: 19,156,485-19,164,234 LOC105379306
    nsv6854337copy number variation1nstd229human GRCh38 chr8: 19,220,501-19,303,300 , GRCh37.p13 chr8: 19,078,011-19,160,811 LOC105379300, LOC100128993, 2 more genes
    nsv6854122copy number variation1nstd229human GRCh38 chr8: 19,210,724-19,676,197 , GRCh37.p13 chr8: 19,068,234-19,533,708 LOC442382, CSGALNACT1, 4 more genes
    nsv6853815copy number variation1nstd229human GRCh38 chr8: 19,041,670-19,378,002 , GRCh37.p13 chr8: 18,899,180-19,235,513 LOC105379301, LOC105379306, 5 more genes
    nsv6852625copy number variation1nstd229human GRCh38 chr8: 18,974,797-19,484,133 , GRCh37.p13 chr8: 18,832,307-19,341,644 LOC105379300, LOC107986868, 8 more genes
    nsv6852404copy number variation1nstd229human GRCh38 chr8: 19,264,528-19,299,234 , GRCh37.p13 chr8: 19,122,038-19,156,745 LOC105379300, LOC105379306
    nsv6850756copy number variation1nstd229human GRCh38 chr8: 19,298,264-19,300,248 , GRCh37.p13 chr8: 19,155,775-19,157,759 LOC105379306
    nsv6847285copy number variation1nstd229human GRCh38 chr8: 19,299,577-19,299,617 , GRCh37.p13 chr8: 19,157,088-19,157,128 LOC105379306
    nsv6846158copy number variation1nstd229human GRCh38 chr8: 19,219,901-20,283,400 , GRCh37.p13 chr8: 19,077,411-20,140,911 LZTS1, LOC100128993, 17 more genes
    nsv6844241copy number variation1nstd229human GRCh38 chr8: 19,284,377-19,388,926 , GRCh37.p13 chr8: 19,141,888-19,246,437 SH2D4A, LOC105379306
    nsv6842540copy number variation1nstd229human GRCh38 chr8: 19,191,912-19,381,034 , GRCh37.p13 chr8: 19,049,422-19,238,545 LOC105379306, LOC105379300, 3 more genes
    nsv6842065copy number variation1nstd229human GRCh38 chr8: 19,291,467-19,330,616 , GRCh37.p13 chr8: 19,148,978-19,188,127 LOC105379306, SH2D4A
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