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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076080inversion1nstd229human GRCh38 chr8: 137,223,456-143,780,837 , GRCh37.p13 chr8: 138,235,699-144,743,525 LOC107986906, FAM83H, 108 more genes
    nsv6871840copy number variation1nstd229human GRCh38 chr8: 143,273,127-143,593,659 , GRCh37.p13 chr8: 144,355,297-144,675,829 MAFA-AS1, SNORD149, 16 more genes
    nsv6865860copy number variation1nstd229human GRCh38 chr8: 143,536,657-143,611,888 , GRCh37.p13 chr8: 144,618,827-144,694,058 LOC100310756, MROH6, 8 more genes
    nsv6860492copy number variation1nstd229human GRCh38 chr8: 143,487,601-143,661,100 , GRCh37.p13 chr8: 144,569,771-144,743,270 MROH6, ZC3H3, 11 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6632504copy number variation1nstd224human GRCh37 chr8: 144,547,942-144,811,340 , GRCh38.p12 chr8: 143,465,772-143,729,170 , GRCh38.p12 chr8|NT_187571.1: 1-206,217 GFUS, ZC3H3, 18 more genes
    nsv6558782inversion1nstd223human GRCh38 chr8: 143,001,224-145,028,420 , GRCh37.p13 chr8: 144,082,641-146,253,806 ZFP41, LY6H, 118 more genes
    nsv6435049copy number variation1nstd223human GRCh38 chr8: 143,430,801-143,727,600 , GRCh37.p13 chr8: 144,512,971-144,743,525 MAFA, MROH6, 19 more genes
    nsv6425791copy number variation1nstd223human GRCh38 chr8: 142,975,701-144,021,300 , GRCh37.p13 chr8: 144,057,118-144,743,525 LY6H, RHPN1-AS1, 55 more genes
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6313487copy number variation1nstd102humanPathogenic GRCh37 chr8: 130,863,093-146,295,771 , GRCh38.p12 chr8: 129,850,847-145,070,385 LOC105375784, CYP11B2, 253 more genes
    nsv6312709copy number variation2nstd102humanPathogenic GRCh37 chr8: 144,295,143-145,701,139 , GRCh38.p12 chr8: 143,213,268-144,475,756 MIR10400, BOP1, 83 more genes
    nsv6312626copy number variation3nstd102humanUncertain significance GRCh37 chr8: 143,822,561-145,743,168 , GRCh38.p12 chr8: 142,741,143-144,517,784 PYCR3, LOC101928902, 110 more genes
    nsv6137256copy number variation1nstd213human GRCh37 chr8: 143,960,000-144,770,001 , GRCh38.p12 chr8: 142,878,584-143,687,831 CYP11B2, GLI4, 38 more genes
    nsv6136342copy number variation1nstd213human GRCh37 chr8: 144,520,000-144,780,001 , GRCh38.p12 chr8: 143,437,830-143,697,831 , GRCh38.p12 chr8|NT_187571.1: 1-174,878 GFUS, ZNF623, 14 more genes
    nsv6136019copy number variation1nstd213human GRCh37 chr8: 144,240,000-144,660,001 , GRCh38.p12 chr8: 143,158,583-143,577,831 NAPRT, LOC100310756, 20 more genes
    nsv6110189inversion1nstd212human GRCh38 chr8: 143,243,347-143,843,862 , GRCh37.p13 chr8: 144,325,517-144,743,525 EEF1D, GLI4, 38 more genes
    nsv5631803insertion1nstd207human GRCh38 chr8: 143,569,279-143,569,279 , GRCh37.p13 chr8: 144,651,449-144,651,449 MROH6
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