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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146375copy number variation1nstd232human GRCh37.p13 chr3: 139,078,019-139,078,109 , GRCh38.p12 chr3: 139,359,177-139,359,267 COPB2
    nsv7144816insertion1nstd232human GRCh37.p13 chr3: 139,087,132-139,087,132 , GRCh38.p12 chr3: 139,368,290-139,368,290 COPB2
    nsv7143135copy number variation1nstd232human GRCh37.p13 chr3: 139,088,207-139,088,294 , GRCh38.p12 chr3: 139,369,365-139,369,452 COPB2
    nsv7142216insertion1nstd232human GRCh37.p13 chr3: 139,088,386-139,088,386 , GRCh38.p12 chr3: 139,369,544-139,369,544 COPB2
    nsv7141726insertion1nstd232human GRCh37.p13 chr3: 139,090,676-139,090,676 , GRCh38.p12 chr3: 139,371,834-139,371,834 COPB2
    nsv7039302inversion1nstd229human GRCh38 chr3: 133,378,933-139,551,784 , GRCh37.p13 chr3: 133,097,777-139,270,626 ESYT3, DONSONP1, 99 more genes
    nsv6736344copy number variation1nstd229human GRCh38 chr3: 139,374,581-139,423,919 , GRCh37.p13 chr3: 139,093,423-139,142,761 COPB2, COPB2-DT
    nsv6735150copy number variation1nstd229human GRCh38 chr3: 139,388,501-139,392,400 , GRCh37.p13 chr3: 139,107,343-139,111,242 COPB2, COPB2-DT
    nsv6732558copy number variation1nstd229human GRCh38 chr3: 139,359,012-139,359,273 , GRCh37.p13 chr3: 139,077,854-139,078,115 COPB2
    nsv6732189copy number variation1nstd229human GRCh38 chr3: 139,357,501-139,360,700 , GRCh37.p13 chr3: 139,076,343-139,079,542 COPB2, MRPS22
    nsv6725094copy number variation1nstd229human GRCh38 chr3: 138,618,667-140,093,940 , GRCh37.p13 chr3: 138,337,509-139,812,782 RPL23AP40, FOXL2NB, 25 more genes
    nsv6720458copy number variation1nstd229human GRCh38 chr3: 139,384,801-139,398,600 , GRCh37.p13 chr3: 139,103,643-139,117,442 COPB2, COPB2-DT
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6561026inversion1nstd223human GRCh38 chr3: 139,386,271-139,387,013 , GRCh37.p13 chr3: 139,105,113-139,105,855 COPB2
    nsv6362129copy number variation1nstd223human GRCh38 chr3: 138,618,667-140,093,940 , GRCh37.p13 chr3: 138,337,509-139,812,782 RBP2, FAIM, 25 more genes
    nsv6311954copy number variation1nstd102humanUncertain significance GRCh37 chr3: 139,062,869-139,108,392 , GRCh38.p12 chr3: 139,344,027-139,389,550 COPB2, COPB2-DT, 1 more genes
    nsv6311778copy number variation1nstd102humanUncertain significance GRCh37 chr3: 137,781,658-139,258,560 , GRCh38.p12 chr3: 138,062,816-139,539,718 PRR23C, ACTG1P1, 29 more genes
    nsv6134785copy number variation1nstd213human GRCh37 chr3: 135,840,000-139,360,001 , GRCh38.p12 chr3: 136,121,158-139,641,159 ACTG1P1, FOXL2, 59 more genes
    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
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