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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5373663translocation1nstd200human GRCh38 chr11: 62,847,118-62,847,118 , GRCh38 chr11: 62,838,160-62,838,160 , GRCh37.p13 chr11: 62,614,590-62,614,590 , GRCh37.p13 chr11: 62,605,632-62,605,632 WDR74
    nsv5373662translocation1nstd200human GRCh38 chr11: 62,850,312-62,850,312 , GRCh38 chr11: 62,837,675-62,837,675 , GRCh37.p13 chr11: 62,605,147-62,605,147 , GRCh37.p13 chr11: 62,617,784-62,617,784 SNHG1, WDR74
    nsv5373661translocation1nstd200human GRCh37.p13 chr11: 62,598,938-62,598,938 , GRCh37.p13 chr11: 62,620,154-62,620,154 , GRCh38 chr11: 62,831,466-62,831,466 , GRCh38 chr11: 62,852,682-62,852,682 STX5, SNORD29, 7 more genes
    nsv5272333copy number variation1nstd204human GRCh38.p13 chr11: 62,830,660-62,837,899 , GRCh37.p13 chr11: 62,598,132-62,605,371 STX5-DT, WDR74, 1 more genes
    nsv5268235copy number variation1nstd204human GRCh38.p13 chr11: 62,664,401-62,843,200 , GRCh37.p13 chr11: 62,431,873-62,610,672 HNRNPUL2, UQCC3, 23 more genes
    nsv5260802copy number variation1nstd204human GRCh38.p13 chr11: 62,838,429-62,845,077 , GRCh37.p13 chr11: 62,605,901-62,612,549 RNU2-2P, WDR74
    nsv5130046mobile element insertion1nstd203human GRCh38 chr11: 62,830,944-62,830,955 , GRCh37.p13 chr11: 62,598,416-62,598,427 STX5, WDR74, 1 more genes
    nsv4830338copy number variation1nstd200human GRCh37 chr11: 62,598,938-62,620,154 , GRCh38.p12 chr11: 62,831,466-62,852,682 SNORD30, STX5-DT, 8 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4612220copy number variation1nstd183human GRCh37 chr11: 62,602,945-62,603,112 , GRCh38.p12 chr11: 62,835,473-62,835,640 WDR74
    nsv4609448copy number variation1nstd183human GRCh37 chr11: 62,601,707-62,602,138 , GRCh38.p12 chr11: 62,834,235-62,834,666 STX5-DT, WDR74
    nsv4456974copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,487,052-62,788,240 , GRCh38.p12 chr11: 62,719,580-63,020,768 RN7SL259P, SNORD29, 29 more genes
    nsv4455787copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,314,663-62,788,240 , GRCh38.p12 chr11: 62,547,191-63,020,768 TTC9C, POLR2G, 48 more genes
    nsv4211953copy number variation1nstd166human GRCh37.p13 chr11: 62,606,147-62,608,706 , GRCh38.p12 chr11: 62,838,675-62,841,234 RNU2-2P, WDR74
    nsv4205552copy number variation1nstd166human GRCh37.p13 chr11: 62,598,868-62,620,099 , GRCh38.p12 chr11: 62,831,396-62,852,627 SNORD22, STX5, 8 more genes
    nsv4195993copy number variation1nstd166human GRCh37.p13 chr11: 62,595,000-62,608,500 , GRCh38.p12 chr11: 62,827,528-62,841,028 WDR74, STX5, 2 more genes
    nsv3963819insertion1nstd168human GRCh38 chr11: 62,839,670-62,849,923 , GRCh37.p13 chr11: 62,607,142-62,617,395 RNU2-2P, WDR74
    nsv3922416copy number variation1nstd102humanPathogenic GRCh38 chr11: 62,433,886-63,096,003 , NCBI36 chr11: 61,957,934-62,620,051 , GRCh37 chr11: 62,201,358-62,863,475 TAF6L, TMEM179B, 51 more genes
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