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Items: 1 to 20 of 136

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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
    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
    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
    nsv4914812copy number variation1nstd200human GRCh38 chr3: 138,639,681-139,021,588 , GRCh37.p13 chr3: 138,358,523-138,740,430 PRR23A, RPL23AP40, 9 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
    nsv4680955copy number variation1nstd189human GRCh37.p13 chr3: 138,044,866-138,867,178 , GRCh38.p12 chr3: 138,326,024-139,148,336 , FOXL2, 18 more genes
    nsv4584853copy number variation1nstd183human GRCh37 chr3: 138,305,900-138,783,114 , GRCh38.p12 chr3: 138,587,058-139,064,272 GAPDHP39, ATP5MC1P3, 12 more genes
    nsv4454433copy number variation1nstd102humanUncertain significance GRCh37 chr3: 138,253,995-138,769,278 , GRCh38.p12 chr3: 138,535,153-139,050,436 RPL23AP40, FOXL2NB, 12 more genes
    nsv4454408copy number variation1nstd102humanUncertain significance GRCh37 chr3: 138,220,588-138,777,135 , GRCh38.p12 chr3: 138,501,746-139,058,293 PRR23B, LINC01391, 12 more genes
    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
    nsv4402455copy number variation1nstd174human GRCh37 chr3: 138,213,166-138,764,229 , GRCh38.p12 chr3: 138,494,324-139,045,387 FAIM, PPIAP72, 12 more genes
    nsv4395611copy number variation1nstd174human GRCh37 chr3: 138,720,204-138,744,939 , GRCh38.p12 chr3: 139,001,362-139,026,097 PRR23A, PRR23B
    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
    nsv4106554copy number variation1nstd166human GRCh37.p13 chr3: 138,707,879-138,740,706 , GRCh38.p12 chr3: 138,989,037-139,021,864 PRR23A, PRR23B
    nsv3923685copy number variation1nstd102humanPathogenic GRCh37 chr3: 137,650,842-144,187,581 , NCBI36 chr3: 139,133,532-145,670,271 , GRCh38 chr3: 137,932,000-144,468,739 ATP1B3, RPL23AP40, 97 more genes
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