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Items: 1 to 20 of 228

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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
    nsv7077239inversion1nstd229human GRCh38 chr8: 28,882,407-30,246,012 , GRCh37.p13 chr8: 28,739,924-30,103,528 LOC105379350, MBOAT4, 27 more genes
    nsv6857778copy number variation1nstd229human GRCh38 chr8: 30,132,301-30,178,000 , GRCh37.p13 chr8: 29,989,817-30,035,516 LEPROTL1, MBOAT4, 1 more genes
    nsv6855251copy number variation1nstd229human GRCh38 chr8: 30,138,190-30,146,669 , GRCh37.p13 chr8: 29,995,706-30,004,185 LEPROTL1, MBOAT4
    nsv6853691copy number variation1nstd229human GRCh38 chr8: 30,147,632-30,148,606 , GRCh37.p13 chr8: 30,005,148-30,006,122 MBOAT4
    nsv6853660copy number variation1nstd229human GRCh38 chr8: 30,132,001-30,136,100 , GRCh37.p13 chr8: 29,989,517-29,993,616 MBOAT4, LEPROTL1
    nsv6851445copy number variation1nstd229human GRCh38 chr8: 29,850,399-30,177,451 , GRCh37.p13 chr8: 29,707,915-30,034,967 DCTN6, RPS15AP24, 8 more genes
    nsv6847423copy number variation1nstd229human GRCh38 chr8: 30,123,650-30,131,410 , GRCh37.p13 chr8: 29,981,166-29,988,926 LEPROTL1, MBOAT4
    nsv6845030copy number variation1nstd229human GRCh38 chr8: 30,147,101-30,150,400 , GRCh37.p13 chr8: 30,004,617-30,007,916 MBOAT4
    nsv6843350copy number variation1nstd229human GRCh38 chr8: 29,796,314-30,528,957 , GRCh37.p13 chr8: 29,653,830-30,386,474 RBPMS, MIR3148, 19 more genes
    nsv6840922copy number variation1nstd229human GRCh38 chr8: 30,141,356-30,165,391 , GRCh37.p13 chr8: 29,998,872-30,022,907 DCTN6, MBOAT4
    nsv6840699copy number variation1nstd229human GRCh38 chr8: 30,137,000-30,138,986 , GRCh37.p13 chr8: 29,994,516-29,996,502 LEPROTL1, MBOAT4
    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
    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
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6571065inversion1nstd223human GRCh38 chr8: 30,135,063-30,135,902 , GRCh37.p13 chr8: 29,992,579-29,993,418 LEPROTL1, MBOAT4
    nsv6565031inversion1nstd223human GRCh38 chr8: 22,900,235-30,247,902 , GRCh37.p13 chr8: 22,757,748-30,105,418 LOC105379349, MIR6876, 140 more genes
    nsv6561507inversion1nstd223human GRCh38 chr8: 30,133,808-30,134,795 , GRCh37.p13 chr8: 29,991,324-29,992,311 MBOAT4, LEPROTL1
    nsv6558340inversion1nstd223human GRCh38 chr8: 28,882,450-30,245,940 , GRCh37.p13 chr8: 28,739,967-30,103,456 LOC105379354, DUSP4, 27 more genes
    nsv6432938copy number variation1nstd223human GRCh38 chr8: 30,147,632-30,148,606 , GRCh37.p13 chr8: 30,005,148-30,006,122 MBOAT4
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