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Items: 1 to 20 of 195

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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
    nsv6852016copy number variation1nstd229human GRCh38 chr8: 41,373,501-41,504,200 , GRCh37.p13 chr8: 41,231,020-41,361,719 GOLGA7, SNORD65B, 1 more genes
    nsv6850449copy number variation1nstd229human GRCh38 chr8: 41,163,697-41,568,923 , GRCh37.p13 chr8: 41,021,216-41,426,442 SFRP1, LOC105379771, 9 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
    nsv6840215copy number variation1nstd229human GRCh38 chr8: 41,486,837-41,488,558 , GRCh37.p13 chr8: 41,344,356-41,346,077 GOLGA7
    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
    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
    nsv6424669copy number variation1nstd223human GRCh38 chr8: 41,436,577-41,517,177 , GRCh37.p13 chr8: 41,294,096-41,374,696 KRT18P37, GOLGA7, 1 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6137284copy number variation1nstd213human GRCh37 chr8: 39,010,000-41,480,001 , GRCh38.p12 chr8: 39,152,481-41,622,482 ADAM3A, ADAM2, 32 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
    nsv6136044copy number variation1nstd213human GRCh37 chr8: 39,020,000-41,480,001 , GRCh38.p12 chr8: 39,162,481-41,622,482 ADAM3A, ADAM2, 31 more genes
    nsv5973938inversion1nstd209human GRCh38 chr8: 41,482,982-43,307,552 , GRCh37.p13 chr8: 41,340,501-43,162,695 , ANK1, 46 more genes
    nsv5919826copy number variation1nstd209human GRCh38 chr8: 41,503,215-41,504,146 , GRCh37.p13 chr8: 41,360,734-41,361,665 GOLGA7
    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
    nsv4960382copy number variation1nstd200human GRCh38 chr8: 41,509,828-41,510,062 , GRCh37.p13 chr8: 41,367,347-41,367,581 GOLGA7, KRT18P37
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