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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5889866copy number variation1nstd209human GRCh38 chr3: 137,097,814-139,588,879 , GRCh37.p13 chr3: 136,816,656-139,307,721 , LOC105374127, 42 more genes
    nsv5685239mobile element insertion1nstd211human GRCh38 chr3: 139,368,117-139,368,117 , GRCh37.p13 chr3: 139,086,959-139,086,959 COPB2
    nsv5396607mobile element insertion1nstd206human GRCh38 chr3: 139,368,117-139,368,168 , GRCh37.p13 chr3: 139,086,959-139,087,010 COPB2
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5097226mobile element insertion1nstd203human GRCh38 chr3: 139,368,108-139,368,117 , GRCh37.p13 chr3: 139,086,950-139,086,959 COPB2
    nsv5089649mobile element insertion1nstd203human GRCh38 chr3: 139,368,103-139,368,117 , GRCh37.p13 chr3: 139,086,945-139,086,959 COPB2
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034922inversion1nstd200human GRCh38 chr3: 137,979,992-148,451,901 , GRCh37.p13 chr3: 137,698,834-148,169,688 , LOC105374148, 132 more genes
    nsv4873274inversion1nstd200human GRCh37 chr3: 137,698,834-148,169,688 , GRCh38.p12 chr3: 137,979,992-148,451,901 , PLSCR5, 132 more genes
    nsv4728141copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,737,687-142,053,396 , GRCh38.p12 chr3: 139,018,845-142,334,554 RNU6-425P, YWHAQP6, 41 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4468743mobile element insertion1nstd166human GRCh37.p13 chr3: 139,102,943-139,102,943 , GRCh38.p12 chr3: 139,384,101-139,384,101 COPB2
    nsv4468742mobile element insertion1nstd166human GRCh37.p13 chr3: 139,086,945-139,086,945 , GRCh38.p12 chr3: 139,368,103-139,368,103 COPB2
    nsv4451778copy number variation1nstd102humanUncertain significance GRCh37 chr3: 135,186,881-140,826,836 , GRCh38.p12 chr3: 135,468,039-141,107,994 ARMC8, EEF1A1P25, 73 more genes
    nsv4347615copy number variation1nstd102humanPathogenic GRCh37 chr3: 135,288,025-146,874,012 , GRCh38.p12 chr3: 135,569,183-147,156,225 RPL6P9, NME9, 145 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv4111429copy number variation1nstd166human GRCh37.p13 chr3: 139,057,000-139,110,000 , GRCh38.p12 chr3: 139,338,158-139,391,158 COPB2, COPB2-DT, 1 more genes
    nsv4105229copy number variation1nstd166human GRCh37.p13 chr3: 139,106,038-139,107,219 , GRCh38.p12 chr3: 139,387,196-139,388,377 COPB2, COPB2-DT
    nsv4092957copy number variation1nstd166human GRCh37.p13 chr3: 139,077,356-139,077,433 , GRCh38.p12 chr3: 139,358,514-139,358,591 COPB2
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