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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055046inversion1nstd229human GRCh38 chr7: 32,752,309-32,780,855 , GRCh37.p13 chr7: 32,791,921-32,820,467 LINC00997
    nsv7040921inversion1nstd229human GRCh38 chr7: 29,656,957-32,757,617 , GRCh37.p13 chr7: 29,696,573-32,797,229 LSM5, RPS27P16, 51 more genes
    nsv6823800copy number variation1nstd229human GRCh38 chr7: 32,761,048-32,776,300 , GRCh37.p13 chr7: 32,800,660-32,815,912 LINC00997
    nsv6823386copy number variation1nstd229human GRCh38 chr7: 32,762,337-32,762,397 , GRCh37.p13 chr7: 32,801,949-32,802,009 LINC00997
    nsv6818174copy number variation1nstd229human GRCh38 chr7: 32,752,301-32,761,000 , GRCh37.p13 chr7: 32,791,913-32,800,612 LINC00997
    nsv6636445copy number variation1nstd102humanPathogenic GRCh37 chr7: 27,133,786-34,466,477 , GRCh38.p12 chr7: 27,094,167-34,426,865 MIR550A1, HOXA-AS3, 119 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6615478copy number variation1nstd223human GRCh38 chr7: 32,725,501-32,769,800 , GRCh37.p13 chr7: 32,765,113-32,809,412 MIR550A2, LINC00997, 2 more genes
    nsv6608555copy number variation1nstd223human GRCh38 chr7: 32,728,801-32,774,500 , GRCh37.p13 chr7: 32,768,413-32,814,112 MIR550A2, ZNRF2P1, 2 more genes
    nsv6606600copy number variation1nstd223human GRCh38 chr7: 32,682,001-32,766,500 , GRCh37.p13 chr7: 32,721,613-32,806,112 MIR550B2, LINC00997, 3 more genes
    nsv6565335inversion1nstd223human GRCh38 chr7: 32,354,819-33,704,107 , GRCh37.p13 chr7: 32,394,431-33,743,719 DPY19L1P1, DPY19L1P2, 20 more genes
    nsv6315453copy number variation1nstd102humanPathogenic GRCh37 chr7: 25,451,740-33,864,069 , GRCh38.p12 chr7: 25,412,121-33,824,457 PLEKHA8, NFE2L3, 141 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313670copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 27,507,832-39,072,473 , GRCh38.p12 chr7: 27,468,213-39,032,873 ADCYAP1R1, AMPH, 175 more genes
    nsv6313493copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 10,745,750-35,305,167 , GRCh38.p12 chr7: 10,706,123-35,265,556 ADCYAP1R1, AHR, 329 more genes
    nsv6266485copy number variation1nstd214human GRCh38 chr7: 32,762,333-32,762,396 , GRCh37.p13 chr7: 32,801,945-32,802,008 LINC00997
    nsv6136989copy number variation1nstd213human GRCh37 chr7: 32,690,000-33,400,001 , GRCh38.p12 chr7: 32,650,388-33,360,389 DPY19L1P1, MIR550B2, 14 more genes
    nsv6135759copy number variation1nstd213human GRCh37 chr7: 32,510,000-33,310,001 , GRCh38.p12 chr7: 32,470,388-33,270,389 RP9, FKBP9, 17 more genes
    nsv6006670copy number variation1nstd212human GRCh38 chr7: 32,729,114-32,760,916 , GRCh37.p13 chr7: 32,768,726-32,800,528 LINC00997, ZNRF2P1, 2 more genes
    nsv6005481copy number variation1nstd212human GRCh38 chr7: 32,762,333-32,762,397 , GRCh37.p13 chr7: 32,801,945-32,802,009 LINC00997
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