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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6118725copy number variation1nstd186human GRCh37 chr1: 153,960,827-153,961,783 , GRCh38.p12 chr1: 153,988,351-153,989,307 RAB13, RPS27
    nsv5873752copy number variation1nstd209human GRCh38 chr1: 153,988,351-153,989,306 , GRCh37.p13 chr1: 153,960,827-153,961,782 RPS27, RAB13
    nsv5570989copy number variation1nstd207human GRCh38 chr1: 153,988,351-153,989,306 , GRCh37.p13 chr1: 153,960,827-153,961,782 RPS27, RAB13
    nsv5422908copy number variation1nstd206human GRCh38 chr1: 153,989,225-153,989,542 , GRCh37.p13 chr1: 153,961,701-153,962,018 RAB13, RPS27
    nsv5422501copy number variation1nstd206human GRCh38 chr1: 153,976,070-153,981,136 , GRCh37.p13 chr1: 153,948,546-153,953,612 RAB13, JTB
    nsv5416401copy number variation1nstd206human GRCh38 chr1: 153,988,351-153,989,307 , GRCh37.p13 chr1: 153,960,827-153,961,783 RPS27, RAB13
    nsv5384551copy number variation1nstd186human GRCh37 chr1: 153,961,223-153,961,489 , GRCh38.p12 chr1: 153,988,747-153,989,013 RAB13, RPS27
    nsv5383695copy number variation1nstd186human GRCh37 chr1: 153,960,968-153,961,591 , GRCh38.p12 chr1: 153,988,492-153,989,115 RPS27, RAB13
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5286623copy number variation1nstd204human GRCh37.p13 chr1: 153,960,901-153,961,778 , GRCh38.p13 chr1: 153,988,425-153,989,302 RAB13, RPS27
    nsv5212209copy number variation1nstd204human GRCh38.p13 chr1: 153,988,350-153,989,376 , GRCh37.p13 chr1: 153,960,826-153,961,852 RAB13, RPS27
    nsv5211686copy number variation1nstd204human GRCh38.p13 chr1: 153,974,901-155,189,600 , GRCh37.p13 chr1: 153,947,377-155,161,231 JTB, PYGO2-AS1, 56 more genes
    nsv5205046copy number variation1nstd204human GRCh38.p13 chr1: 153,988,401-153,989,300 , GRCh37.p13 chr1: 153,960,877-153,961,776 RAB13, RPS27
    nsv5064755mobile element insertion1nstd203human GRCh38 chr1: 153,987,515-153,987,534 , GRCh37.p13 chr1: 153,959,991-153,960,010 RAB13
    nsv4903898copy number variation1nstd200human GRCh38 chr1: 153,891,283-154,169,965 , GRCh37.p13 chr1: 153,863,759-154,142,441 DENND4B, RN7SL431P, 15 more genes
    nsv4897482copy number variation1nstd200human GRCh38 chr1: 153,988,305-153,989,422 , GRCh37.p13 chr1: 153,960,781-153,961,898 RAB13, RPS27
    nsv4784265copy number variation1nstd200human GRCh37 chr1: 153,961,221-153,961,490 , GRCh38.p12 chr1: 153,988,745-153,989,014 RPS27, RAB13
    nsv4781207copy number variation1nstd200human GRCh37 chr1: 153,863,759-154,142,441 , GRCh38.p12 chr1: 153,891,283-154,169,965 MIR6737, SLC39A1, 15 more genes
    nsv4774036mobile element deletion1nstd200human GRCh37 chr1: 153,961,613-153,962,053 , GRCh38.p12 chr1: 153,989,137-153,989,577 RPS27, RAB13
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
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