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Items: 1 to 20 of 226

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137911insertion1nstd232human GRCh37.p13 chr7: 33,014,373-33,014,373 , GRCh38.p12 chr7: 32,974,761-32,974,761 FKBP9
    nsv6833981copy number variation1nstd229human GRCh38 chr7: 33,007,210-33,008,554 , GRCh37.p13 chr7: 33,046,822-33,048,166 FKBP9
    nsv6825887copy number variation1nstd229human GRCh38 chr7: 32,959,936-33,014,921 , GRCh37.p13 chr7: 32,999,548-33,054,533 FKBP9, NT5C3A, 1 more genes
    nsv6823192copy number variation1nstd229human GRCh38 chr7: 32,966,872-32,969,418 , GRCh37.p13 chr7: 33,006,484-33,009,030 FKBP9
    nsv6820997copy number variation1nstd229human GRCh38 chr7: 32,984,241-32,984,277 , GRCh37.p13 chr7: 33,023,853-33,023,889 FKBP9
    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
    nsv6603676copy number variation1nstd223human GRCh38 chr7: 32,962,195-32,965,627 , GRCh37.p13 chr7: 33,001,807-33,005,239 FKBP9
    nsv6600322copy number variation1nstd223human GRCh38 chr7: 33,007,208-33,008,551 , GRCh37.p13 chr7: 33,046,820-33,048,163 FKBP9
    nsv6565335inversion1nstd223human GRCh38 chr7: 32,354,819-33,704,107 , GRCh37.p13 chr7: 32,394,431-33,743,719 DPY19L1P1, DPY19L1P2, 20 more genes
    nsv6556652inversion1nstd223human GRCh38 chr7: 32,865,301-34,895,818 , GRCh37.p13 chr7: 32,904,913-34,935,430 RP9P, RPS29P14, 17 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
    nsv6169596copy number variation1nstd214human GRCh38 chr7: 32,992,254-32,992,332 , GRCh37.p13 chr7: 33,031,866-33,031,944 FKBP9
    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
    nsv6012860copy number variation1nstd212human GRCh38 chr7: 32,965,803-32,965,854 , GRCh37.p13 chr7: 33,005,415-33,005,466 FKBP9
    nsv5924528copy number variation1nstd209human GRCh38 chr7: 33,007,208-33,008,550 , GRCh37.p13 chr7: 33,046,820-33,048,162 FKBP9
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