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Items: 1 to 20 of 173

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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
    nsv7070960inversion1nstd229human GRCh38 chr8: 27,006,998-27,104,574 , GRCh37.p13 chr8: 26,864,515-26,962,091 LOC100132229, MIR548H4
    nsv7067235inversion1nstd229human GRCh38 chr8: 27,018,106-27,100,814 , GRCh37.p13 chr8: 26,875,623-26,958,331 MIR548H4
    nsv6842056copy number variation1nstd229human GRCh38 chr8: 27,042,701-27,049,000 , GRCh37.p13 chr8: 26,900,218-26,906,517 MIR548H4
    nsv6840987copy number variation1nstd229human GRCh38 chr8: 27,045,823-27,052,768 , GRCh37.p13 chr8: 26,903,340-26,910,285 MIR548H4
    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
    nsv6420574copy number variation1nstd223human GRCh38 chr8: 27,045,823-27,052,765 , GRCh37.p13 chr8: 26,903,340-26,910,282 MIR548H4
    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
    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
    nsv6136028copy number variation1nstd213human GRCh37 chr8: 25,020,000-26,990,001 , GRCh38.p12 chr8: 25,162,485-27,132,484 ADRA1A, BNIP3L, 27 more genes
    nsv5919019copy number variation1nstd209human GRCh38 chr8: 26,939,516-27,553,947 , GRCh37.p13 chr8: 26,797,033-27,411,464 LOC105379339, TRIM35, 9 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
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
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