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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7065639inversion1nstd229human GRCh38 chr8: 40,079,981-42,715,940 , GRCh37.p13 chr8: 39,937,500-42,571,083 LOC105379390, RPL17P30, 44 more genes
    nsv7062022inversion1nstd229human GRCh38 chr8: 41,644,817-41,655,175 , GRCh37.p13 chr8: 41,502,336-41,512,694 ANK1, NKX6-3
    nsv6852035copy number variation1nstd229human GRCh38 chr8: 41,602,240-41,710,755 , GRCh37.p13 chr8: 41,459,759-41,568,273 NKX6-3, ANK1, 3 more genes
    nsv6846011copy number variation1nstd229human GRCh38 chr8: 40,859,599-41,864,333 , GRCh37.p13 chr8: 40,717,118-41,721,851 MIR548AO, LOC105379392, 20 more genes
    nsv6840448copy number variation1nstd229human GRCh38 chr8: 41,508,501-41,922,600 , GRCh37.p13 chr8: 41,366,020-41,780,118 ANK1, GPAT4, 9 more genes
    nsv6636422copy number variation1nstd102humanUncertain significance GRCh37 chr8: 41,455,579-41,568,924 , GRCh38.p12 chr8: 41,598,060-41,711,406 ANK1, GPAT4, 3 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6632987copy number variation1nstd224human GRCh37 chr8: 41,161,759-41,615,138 , GRCh38.p12 chr8: 41,304,240-41,757,620 ANK1, NKX6-3, 10 more genes
    nsv6427545copy number variation1nstd223human GRCh38 chr8: 41,638,389-41,646,931 , GRCh37.p13 chr8: 41,495,908-41,504,450 NKX6-3
    nsv6424882copy number variation1nstd223human GRCh38 chr8: 41,478,312-41,920,906 , GRCh37.p13 chr8: 41,335,831-41,778,424 GPAT4-AS1, RN7SL149P, 9 more genes
    nsv6420240copy number variation1nstd223human GRCh38 chr8: 41,643,556-41,644,230 , GRCh37.p13 chr8: 41,501,075-41,501,749 NKX6-3
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6137289copy number variation1nstd213human GRCh37 chr8: 41,380,000-41,900,001 , GRCh38.p12 chr8: 41,522,481-42,042,483 ANK1, KAT6A, 8 more genes
    nsv6136047copy number variation1nstd213human GRCh37 chr8: 41,160,000-42,320,001 , GRCh38.p12 chr8: 41,302,481-42,462,483 SLC20A2, GOLGA7, 27 more genes
    nsv6013572copy number variation1nstd212human GRCh38 chr8: 41,651,004-41,651,056 , GRCh37.p13 chr8: 41,508,523-41,508,575 NKX6-3
    nsv6008366copy number variation1nstd212human GRCh38 chr8: 41,646,910-41,646,975 , GRCh37.p13 chr8: 41,504,429-41,504,494 NKX6-3
    nsv5973938inversion1nstd209human GRCh38 chr8: 41,482,982-43,307,552 , GRCh37.p13 chr8: 41,340,501-43,162,695 , ANK1, 46 more genes
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 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
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