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Items: 1 to 20 of 155

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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
    nsv5443886copy number variation1nstd206human GRCh38 chr3: 138,480,477-138,945,708 , GRCh37.p13 chr3: 138,199,319-138,664,550 ESYT3, GAPDHP39, 10 more genes
    nsv5440706copy number variation1nstd206human GRCh38 chr3: 138,941,389-138,941,697 , GRCh37.p13 chr3: 138,660,231-138,660,539 LINC01391
    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
    nsv5318504copy number variation1nstd204human GRCh38.p13 chr3: 138,574,740-138,957,438 , GRCh37.p13 chr3: 138,293,582-138,676,280 FAIM, ATP5MC1P3, 9 more genes
    nsv5224079copy number variation1nstd204human GRCh38.p13 chr3: 138,891,805-138,954,903 , GRCh37.p13 chr3: 138,610,647-138,673,745 FOXL2NB, LINC01391, 1 more genes
    nsv5223349copy number variation1nstd204human GRCh38.p13 chr3: 138,574,801-138,956,600 , GRCh37.p13 chr3: 138,293,643-138,675,442 PPIAP72, EEF1A1P25, 9 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
    nsv4914811copy number variation1nstd200human GRCh38 chr3: 138,574,749-138,957,430 , GRCh37.p13 chr3: 138,293,591-138,676,272 FOXL2, PPIAP72, 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
    nsv4804839copy number variation1nstd200human GRCh37 chr3: 138,293,591-138,676,272 , GRCh38.p12 chr3: 138,574,749-138,957,430 LINC01391, CEP70, 9 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
    nsv4674245copy number variation1nstd102humanLikely benign GRCh37 chr3: 138,203,261-138,669,628 , GRCh38.p12 chr3: 138,484,419-138,950,786 FOXL2NB, LINC01391, 9 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
    nsv4452205copy number variation1nstd102humanUncertain significance GRCh37 chr3: 138,439,305-138,660,471 , GRCh38.p12 chr3: 138,720,463-138,941,629 ATP5MC1P3, GAPDHP39, 4 more genes
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