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Items: 1 to 20 of 368

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072719inversion1nstd229human GRCh38 chr9: 14,792,079-19,156,478 , GRCh37.p13 chr9: 14,792,077-19,156,476 RN7SL98P, RRAGA, 49 more genes
    nsv7068293inversion1nstd229human GRCh38 chr9: 12,453,912-21,375,878 , GRCh37.p13 chr9: 12,453,912-21,375,877 RNU6-264P, PSMC3P1, 115 more genes
    nsv7067412inversion1nstd229human GRCh38 chr9: 19,125,661-19,160,987 , GRCh37.p13 chr9: 19,125,659-19,160,985 PLIN2
    nsv7062404inversion1nstd229human GRCh38 chr9: 12,646,715-21,082,028 , GRCh37.p13 chr9: 12,646,715-21,082,027 RPS6, RPL7AP47, 95 more genes
    nsv6878050copy number variation1nstd229human GRCh38 chr9: 19,116,651-19,118,320 , GRCh37.p13 chr9: 19,116,649-19,118,318 PLIN2
    nsv6877415copy number variation1nstd229human GRCh38 chr9: 18,863,175-19,659,789 , GRCh37.p13 chr9: 18,863,173-19,659,787 ACER2, ADAMTSL1, 15 more genes
    nsv6875435copy number variation1nstd229human GRCh38 chr9: 19,111,196-19,130,187 , GRCh37.p13 chr9: 19,111,194-19,130,185 PLIN2
    nsv6874543copy number variation1nstd229human GRCh38 chr9: 19,109,689-19,111,366 , GRCh37.p13 chr9: 19,109,687-19,111,364 PLIN2
    nsv6874370copy number variation1nstd229human GRCh38 chr9: 19,077,797-19,550,661 , GRCh37.p13 chr9: 19,077,795-19,550,659 RPS6P10, MAP1LC3BP1, 8 more genes
    nsv6871939copy number variation1nstd229human GRCh38 chr9: 19,124,948-19,128,222 , GRCh37.p13 chr9: 19,124,946-19,128,220 PLIN2
    nsv6871453copy number variation1nstd229human GRCh38 chr9: 19,105,701-19,115,600 , GRCh37.p13 chr9: 19,105,699-19,115,598 PLIN2
    nsv6868719copy number variation1nstd229human GRCh38 chr9: 19,121,165-19,123,564 , GRCh37.p13 chr9: 19,121,163-19,123,562 PLIN2
    nsv6867768copy number variation1nstd229human GRCh38 chr9: 17,165,352-20,022,245 , GRCh37.p13 chr9: 17,165,350-20,022,243 SH3GL2, SLC24A2, 31 more genes
    nsv6867175copy number variation1nstd229human GRCh38 chr9: 19,125,463-19,509,652 , GRCh37.p13 chr9: 19,125,461-19,509,650 PLIN2, ACER2, 7 more genes
    nsv6866531copy number variation1nstd229human GRCh38 chr9: 19,116,262-19,229,910 , GRCh37.p13 chr9: 19,116,260-19,229,908 PLIN2, RPS6P10, 1 more genes
    nsv6864776copy number variation1nstd229human GRCh38 chr9: 19,103,650-19,109,375 , GRCh37.p13 chr9: 19,103,648-19,109,373 PLIN2
    nsv6864332copy number variation1nstd229human GRCh38 chr9: 19,113,101-19,183,800 , GRCh37.p13 chr9: 19,113,099-19,183,798 PLIN2
    nsv6863740copy number variation1nstd229human GRCh38 chr9: 19,089,211-19,375,587 , GRCh37.p13 chr9: 19,089,209-19,375,585 RPS6, RPS6P10, 3 more genes
    nsv6863278copy number variation1nstd229human GRCh38 chr9: 19,106,686-19,110,536 , GRCh37.p13 chr9: 19,106,684-19,110,534 PLIN2
    nsv6861485copy number variation1nstd229human GRCh38 chr9: 19,080,401-19,156,700 , GRCh37.p13 chr9: 19,080,399-19,156,698 HAUS6, PLIN2
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