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Items: 1 to 20 of 188

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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
    nsv6852450copy number variation1nstd229human GRCh38 chr8: 29,331,301-29,395,800 , GRCh37.p13 chr8: 29,188,818-29,253,317 LOC105379349, DUSP4
    nsv6848784copy number variation1nstd229human GRCh38 chr8: 29,329,901-29,549,200 , GRCh37.p13 chr8: 29,187,418-29,406,717 LOC107986883, LOC105379349, 3 more genes
    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
    nsv6565031inversion1nstd223human GRCh38 chr8: 22,900,235-30,247,902 , GRCh37.p13 chr8: 22,757,748-30,105,418 LOC105379349, MIR6876, 140 more genes
    nsv6562400inversion1nstd223human GRCh38 chr8: 29,331,548-29,332,187 , GRCh37.p13 chr8: 29,189,065-29,189,704 DUSP4
    nsv6558340inversion1nstd223human GRCh38 chr8: 28,882,450-30,245,940 , GRCh37.p13 chr8: 28,739,967-30,103,456 LOC105379354, DUSP4, 27 more genes
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 LOC101928016, RPL23AP54, 568 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6137272copy number variation1nstd213human GRCh37 chr8: 26,370,000-35,590,001 , GRCh38.p12 chr8: 26,512,484-35,732,483 ADRA1A, CHRNA2, 141 more genes
    nsv6137044copy number variation1nstd213human GRCh37 chr8: 12,460,000-33,310,001 , GRCh38.p12 chr8: 12,602,491-33,452,483 NAT1, ASAH1, 322 more genes
    nsv6136655copy number variation1nstd213human GRCh37 chr8: 19,630,000-29,910,001 , GRCh38.p12 chr8: 19,772,489-30,052,485 BMP1, BNIP3L, 194 more genes
    nsv6136573copy number variation1nstd213human GRCh37 chr8: 25,790,000-30,640,001 , GRCh38.p12 chr8: 25,932,484-30,782,485 EPHX2, GSR, 99 more genes
    nsv6136032copy number variation1nstd213human GRCh37 chr8: 29,170,000-29,390,001 , GRCh38.p12 chr8: 29,312,483-29,532,484 DUSP4, LOC105379349, 3 more genes
    nsv6136029copy number variation1nstd213human GRCh37 chr8: 26,360,000-35,600,001 , GRCh38.p12 chr8: 26,502,484-35,742,483 ADRA1A, CHRNA2, 141 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4959922copy number variation1nstd200human GRCh38 chr8: 29,342,671-29,343,570 , GRCh37.p13 chr8: 29,200,188-29,201,087 DUSP4
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