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Items: 1 to 20 of 270

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5888931copy number variation1nstd209human GRCh38 chr5: 139,581,522-139,581,621 , GRCh37.p13 chr5: 138,961,107-138,961,206 UBE2D2
    nsv5693370mobile element insertion1nstd211human GRCh38 chr5: 139,597,077-139,597,077 , GRCh37.p13 chr5: 138,976,662-138,976,662 UBE2D2
    nsv5690663mobile element insertion1nstd211human GRCh38 chr5: 139,620,619-139,620,619 , GRCh37.p13 chr5: 139,000,204-139,000,204 UBE2D2
    nsv5566074copy number variation1nstd207human GRCh38 chr5: 139,581,522-139,581,621 , GRCh37.p13 chr5: 138,961,107-138,961,206 UBE2D2
    nsv5543931insertion1nstd206human GRCh38 chr5: 139,620,619-139,620,670 , GRCh37.p13 chr5: 139,000,204-139,000,255 UBE2D2
    nsv5472363copy number variation1nstd206human GRCh38 chr5: 139,597,969-139,598,135 , GRCh37.p13 chr5: 138,977,554-138,977,720 UBE2D2
    nsv5458698copy number variation1nstd206human GRCh38 chr5: 139,581,524-139,581,622 , GRCh37.p13 chr5: 138,961,109-138,961,207 UBE2D2
    nsv5457213copy number variation1nstd206human GRCh38 chr5: 139,602,939-139,603,045 , GRCh37.p13 chr5: 138,982,524-138,982,630 UBE2D2
    nsv5454082copy number variation1nstd206human GRCh38 chr5: 139,577,421-139,579,023 , GRCh37.p13 chr5: 138,957,006-138,958,608 UBE2D2
    nsv5411181mobile element insertion1nstd206human GRCh38 chr5: 139,597,077-139,597,080 , GRCh37.p13 chr5: 138,976,662-138,976,665 UBE2D2
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5378110translocation1nstd200human GRCh38 chr5: 139,602,939-139,602,939 , GRCh38 chr5: 139,603,045-139,603,045 , GRCh37.p13 chr5: 138,982,524-138,982,524 , GRCh37.p13 chr5: 138,982,630-138,982,630 UBE2D2
    nsv5325776translocation1nstd204human GRCh38.p13 chr5: 139,581,622-139,581,622 , GRCh38.p13 chr5: 139,581,524-139,581,524 , GRCh37.p13 chr5: 138,961,207-138,961,207 , GRCh37.p13 chr5: 138,961,109-138,961,109 UBE2D2
    nsv5313114copy number variation1nstd204human GRCh37.p13 chr5: 138,988,462-138,992,917 , GRCh38.p13 chr5: 139,608,877-139,613,332 UBE2D2, HSPE1P15, 1 more genes
    nsv5240084copy number variation1nstd204human GRCh38.p13 chr5: 139,588,863-139,590,862 , GRCh37.p13 chr5: 138,968,448-138,970,447 UBE2D2
    nsv5223559copy number variation1nstd204human GRCh38.p13 chr5: 139,608,852-139,613,349 , GRCh37.p13 chr5: 138,988,437-138,992,934 H3P25, UBE2D2, 1 more genes
    nsv5096973mobile element insertion1nstd203human GRCh38 chr5: 139,620,603-139,620,619 , GRCh37.p13 chr5: 139,000,188-139,000,204 UBE2D2
    nsv5093672mobile element insertion1nstd203human GRCh38 chr5: 139,597,067-139,597,077 , GRCh37.p13 chr5: 138,976,652-138,976,662 UBE2D2
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
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