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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968271insertion1nstd209human GRCh38 chr15: 43,334,633-43,334,633 , GRCh37.p13 chr15: 43,626,831-43,626,831 ADAL
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5150529mobile element insertion1nstd203human GRCh38 chr15: 43,347,704-43,347,716 , GRCh37.p13 chr15: 43,639,902-43,639,914 ADAL
    nsv5140984mobile element insertion1nstd203human GRCh38 chr15: 43,334,153-43,334,171 , GRCh37.p13 chr15: 43,626,351-43,626,369 ADAL
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005327copy number variation1nstd200human GRCh38 chr15: 43,352,096-43,393,954 , GRCh37.p13 chr15: 43,644,294-43,686,152 TUBGCP4, RN7SL487P, 2 more genes
    nsv5005326copy number variation1nstd200human GRCh38 chr15: 43,351,993-43,352,159 , GRCh37.p13 chr15: 43,644,191-43,644,357 ADAL
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4863762copy number variation1nstd200human GRCh37 chr15: 43,644,294-43,686,152 , GRCh38.p12 chr15: 43,352,096-43,393,954 TUBGCP4, ZSCAN29, 2 more genes
    nsv4729554copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 43,135,272-43,744,542 , GRCh38.p12 chr15: 42,843,074-43,452,344 EPB42, FDPSP4, 16 more genes
    nsv4675221copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,420,601-44,198,616 , GRCh38.p12 chr15: 43,128,403-43,906,418 TGM5, CATSPER2P1, 38 more genes
    nsv4674906copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,017,718-43,685,171 , GRCh38.p12 chr15: 42,725,520-43,392,973 UBR1, CDAN1, 17 more genes
    nsv4555711insertion1nstd166human GRCh37.p13 chr15: 43,626,351-43,626,351 , GRCh38.p12 chr15: 43,334,153-43,334,153 ADAL
    nsv4457111copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,062,580-43,744,411 , GRCh38.p12 chr15: 42,770,382-43,452,213 CCNDBP1, TUBGCP4, 17 more genes
    nsv4456911copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,118,272-43,668,969 , GRCh38.p12 chr15: 42,826,074-43,376,771 CCNDBP1, TMEM62, 14 more genes
    nsv4456301copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,062,580-43,737,484 , GRCh38.p12 chr15: 42,770,382-43,445,286 LCMT2, TMEM62, 17 more genes
    nsv4455895copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,277,078-43,634,358 , GRCh38.p12 chr15: 42,984,880-43,342,160 TGM5, SPCS2P1, 10 more genes
    nsv4252418copy number variation1nstd166human GRCh37.p13 chr15: 43,644,341-43,686,152 , GRCh38.p12 chr15: 43,352,143-43,393,954 ADAL, RN7SL487P, 2 more genes
    nsv4240288copy number variation1nstd166human GRCh37.p13 chr15: 43,634,483-43,634,945 , GRCh38.p12 chr15: 43,342,285-43,342,747 ADAL
    nsv4235617copy number variation1nstd166human GRCh37.p13 chr15: 43,622,759-43,622,810 , GRCh38.p12 chr15: 43,330,561-43,330,612 LCMT2, ADAL
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