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Items: 1 to 20 of 469

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7061563inversion1nstd229human GRCh38 chr8: 27,492,341-29,312,113 , GRCh37.p13 chr8: 27,349,858-29,169,630 LOC100130612, HMBOX1, 37 more genes
    nsv6857117copy number variation1nstd229human GRCh38 chr8: 28,424,898-28,430,950 , GRCh37.p13 chr8: 28,282,415-28,288,467 FBXO16
    nsv6856913copy number variation1nstd229human GRCh38 chr8: 28,445,215-28,450,893 , GRCh37.p13 chr8: 28,302,732-28,308,410 FBXO16
    nsv6856610copy number variation1nstd229human GRCh38 chr8: 28,459,029-28,489,087 , GRCh37.p13 chr8: 28,316,546-28,346,604 FBXO16
    nsv6852408copy number variation1nstd229human GRCh38 chr8: 28,439,468-28,441,497 , GRCh37.p13 chr8: 28,296,985-28,299,014 FBXO16
    nsv6850395copy number variation1nstd229human GRCh38 chr8: 28,404,697-28,433,446 , GRCh37.p13 chr8: 28,262,214-28,290,963 RNU6-178P, FBXO16
    nsv6849019copy number variation1nstd229human GRCh38 chr8: 28,445,579-28,448,178 , GRCh37.p13 chr8: 28,303,096-28,305,695 FBXO16
    nsv6847634copy number variation1nstd229human GRCh38 chr8: 28,376,752-28,543,566 , GRCh37.p13 chr8: 28,234,269-28,401,083 RNA5SP259, MIR4288, 4 more genes
    nsv6847209copy number variation1nstd229human GRCh38 chr8: 28,443,201-28,444,700 , GRCh37.p13 chr8: 28,300,718-28,302,217 FBXO16
    nsv6846102copy number variation1nstd229human GRCh38 chr8: 28,240,525-28,452,092 , GRCh37.p13 chr8: 28,098,042-28,309,609 RNU6-178P, RPL5P22, 3 more genes
    nsv6845678copy number variation1nstd229human GRCh38 chr8: 28,470,620-28,616,160 , GRCh37.p13 chr8: 28,328,137-28,473,677 MIR4288, RNA5SP259, 3 more genes
    nsv6841526copy number variation1nstd229human GRCh38 chr8: 28,453,201-28,455,000 , GRCh37.p13 chr8: 28,310,718-28,312,517 FBXO16
    nsv6840162copy number variation1nstd229human GRCh38 chr8: 28,488,444-28,491,563 , GRCh37.p13 chr8: 28,345,961-28,349,080 FBXO16
    nsv6839985copy number variation1nstd229human GRCh38 chr8: 28,051,949-30,854,206 , GRCh37.p13 chr8: 27,909,466-30,711,722 PPP2CB, RNU6-1218P, 59 more genes
    nsv6839334copy number variation1nstd229human GRCh38 chr8: 28,454,007-28,454,728 , GRCh37.p13 chr8: 28,311,524-28,312,245 FBXO16
    nsv6839249copy number variation1nstd229human GRCh38 chr8: 28,428,001-28,436,200 , GRCh37.p13 chr8: 28,285,518-28,293,717 FBXO16
    nsv6838536copy number variation1nstd229human GRCh38 chr8: 28,486,503-28,487,539 , GRCh37.p13 chr8: 28,344,020-28,345,056 FBXO16
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6636640copy number variation1nstd102humanUncertain significance GRCh37 chr8: 27,064,033-28,832,392 , GRCh38.p12 chr8: 27,206,516-28,974,875 ZNF395, PNOC, 39 more genes
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