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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112738copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,619-3,951,208 , GRCh38.p12 chr6: 149,619-3,950,974 LINC01600, TUBB2BP1, 66 more genes
    nsv5844607copy number variation1nstd209human GRCh38 chr6: 3,154,566-3,163,486 , GRCh37.p13 chr6: 3,154,800-3,163,720 LOC105374889, TUBB2A
    nsv5381385copy number variation2nstd102humanUncertain significance GRCh37 chr6: 2,833,842-3,227,777 , GRCh38.p12 chr6: 2,833,608-3,227,543 SERPINB9-AS1, RIPK1, 20 more genes
    nsv5232448copy number variation1nstd204human GRCh38.p13 chr6: 3,153,466-3,163,311 , GRCh37.p13 chr6: 3,153,700-3,163,545 BPHL, LOC105374889, 1 more genes
    nsv4729315copy number variation1nstd102humanPathogenic GRCh37 chr6: 302,183-3,290,583 , GRCh38.p12 chr6: 302,183-3,290,349 RIPK1, MARK2P18, 53 more genes
    nsv4675760copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,157,162-3,233,433 , GRCh38.p12 chr6: 3,156,928-3,233,199 TUBB2A, TUBB2BP1, 4 more genes
    nsv4598499copy number variation1nstd183human GRCh37 chr6: 3,156,630-3,177,909 , GRCh38.p12 chr6: 3,156,396-3,177,675 TUBB2BP1, LOC105374889, 1 more genes
    nsv4593504copy number variation1nstd183human GRCh37 chr6: 3,157,776-3,162,121 , GRCh38.p12 chr6: 3,157,542-3,161,887 LOC105374889, TUBB2A
    nsv4592415copy number variation1nstd183human GRCh37 chr6: 3,156,630-3,166,931 , GRCh38.p12 chr6: 3,156,396-3,166,697 TUBB2A, LOC105374889
    nsv4457099copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,157,235-3,218,178 , GRCh38.p12 chr6: 3,157,001-3,217,944 TUBB2A, LINC02525, 2 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4455280copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,151,303-3,220,269 , GRCh38.p12 chr6: 3,151,069-3,220,035 BPHL, TUBB2BP1, 3 more genes
    nsv4409225copy number variation1nstd174human GRCh37 chr6: 3,157,163-3,223,513 , GRCh38.p12 chr6: 3,156,929-3,223,279 LOC105374889, TUBB2A, 3 more genes
    nsv4394946copy number variation1nstd174human GRCh37 chr6: 3,155,668-3,181,359 , GRCh38.p12 chr6: 3,155,434-3,181,125 TUBB2BP1, LOC105374889, 2 more genes
    nsv4371355copy number variation1nstd173human GRCh37 chr6: 3,157,163-3,233,433 , GRCh38.p12 chr6: 3,156,929-3,233,199 TUBB2A, TUBB2B, 4 more genes
    nsv4369920copy number variation1nstd173human GRCh37 chr6: 3,157,163-3,232,759 , GRCh38.p12 chr6: 3,156,929-3,232,525 TUBB2B, LINC02525, 4 more genes
    nsv4132155copy number variation1nstd166human GRCh37.p13 chr6: 3,156,950-3,179,500 , GRCh38.p12 chr6: 3,156,716-3,179,266 TUBB2A, TUBB2BP1, 1 more genes
    nsv3923249copy number variation1nstd102humanPathogenic NCBI36 chr6: 110,675-8,981,266 , GRCh38 chr6: 165,675-9,036,034 , GRCh37 chr6: 165,675-9,036,267 LOC100506207, LOC105374889, 148 more genes
    nsv3923206copy number variation1nstd102humanPathogenic NCBI36 chr6: 108,083-3,404,840 , GRCh38 chr6: 163,083-3,459,607 , GRCh37 chr6: 163,083-3,459,841 LOC105374883, MIR4645, 58 more genes
    nsv3922576copy number variation1nstd102humanPathogenic GRCh37 chr6: 164,633-6,284,470 , GRCh38 chr6: 164,633-6,284,237 , NCBI36 chr6: 109,633-6,229,469 GLRX3P2, CDYL, 106 more genes
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