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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979257insertion1nstd209human GRCh38 chr20: 25,322,381-25,322,381 , GRCh37.p13 chr20: 25,303,017-25,303,017 ABHD12
    nsv5960629copy number variation1nstd209human GRCh38 chr20: 24,517,514-25,490,454 , GRCh37.p13 chr20: 24,498,150-25,471,090 LOC105372581, LOC107985402, 18 more genes
    nsv5707019mobile element insertion1nstd211human GRCh38 chr20: 25,335,491-25,335,491 , GRCh37.p13 chr20: 25,316,127-25,316,127 ABHD12
    nsv5673416copy number variation1nstd102humanPathogenic GRCh37 chr20: 25,295,561-25,300,954 , GRCh38.p12 chr20: 25,314,925-25,320,318 ABHD12
    nsv5673177copy number variation1nstd102humanPathogenic GRCh37 chr20: 25,371,129-25,371,339 , GRCh38.p12 chr20: 25,390,493-25,390,703 ABHD12
    nsv5593500copy number variation1nstd207human GRCh38 chr20: 25,359,191-25,361,724 , GRCh37.p13 chr20: 25,339,827-25,342,360 ABHD12
    nsv5564320copy number variation1nstd102humanUncertain significance GRCh37 chr20: 25,281,481-25,290,231 , GRCh38.p12 chr20: 25,300,845-25,309,595 ABHD12
    nsv5533912copy number variation1nstd206human GRCh38 chr20: 25,359,177-25,361,746 , GRCh37.p13 chr20: 25,339,813-25,342,382 ABHD12
    nsv5530717copy number variation1nstd206human GRCh38 chr20: 25,121,452-25,367,703 , GRCh37.p13 chr20: 25,102,088-25,348,339 ENTPD6, PYGB, 6 more genes
    nsv5528147copy number variation1nstd206human GRCh38 chr20: 25,348,851-25,359,149 , GRCh37.p13 chr20: 25,329,487-25,339,785 ABHD12
    nsv5522959copy number variation1nstd206human GRCh38 chr20: 25,343,046-25,362,952 , GRCh37.p13 chr20: 25,323,682-25,343,588 ABHD12
    nsv5515718copy number variation1nstd206human GRCh38 chr20: 25,341,532-25,341,609 , GRCh37.p13 chr20: 25,322,168-25,322,245 ABHD12
    nsv5350240translocation1nstd200human GRCh38 chr20: 25,341,609-25,341,609 , GRCh38 chr20: 25,341,532-25,341,532 , GRCh37.p13 chr20: 25,322,245-25,322,245 , GRCh37.p13 chr20: 25,322,168-25,322,168 ABHD12
    nsv5342741translocation1nstd200human GRCh37 chr20: 25,322,168-25,322,168 , GRCh37 chr20: 25,322,245-25,322,245 , GRCh38.p12 chr20: 25,341,532-25,341,532 , GRCh38.p12 chr20: 25,341,609-25,341,609 ABHD12
    nsv5323867copy number variation1nstd204human GRCh37.p13 chr20: 25,275,308-25,275,684 , GRCh38.p13 chr20: 25,294,672-25,295,048 PYGB, ABHD12
    nsv5320418translocation1nstd204human GRCh38.p13 chr20: 25,341,532-25,341,532 , GRCh38.p13 chr20: 25,341,609-25,341,609 , GRCh37.p13 chr20: 25,322,245-25,322,245 , GRCh37.p13 chr20: 25,322,168-25,322,168 ABHD12
    nsv5299687copy number variation1nstd204human GRCh38.p13 chr20: 25,332,901-25,333,500 , GRCh37.p13 chr20: 25,313,537-25,314,136 ABHD12
    nsv5193207mobile element insertion1nstd203human GRCh38 chr20: 25,313,630-25,313,630 , GRCh37.p13 chr20: 25,294,266-25,294,266 ABHD12
    nsv5191529mobile element insertion1nstd203human GRCh38 chr20: 25,313,578-25,313,578 , GRCh37.p13 chr20: 25,294,214-25,294,214 ABHD12
    nsv5171802mobile element insertion1nstd203human GRCh38 chr20: 25,387,590-25,387,608 , GRCh37.p13 chr20: 25,368,226-25,368,244 ABHD12
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