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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057873inversion1nstd229human GRCh38 chr7: 29,679,024-30,286,151 , GRCh37.p13 chr7: 29,718,640-30,325,767 SCRN1, LOC105375217, 13 more genes
    nsv7050299inversion1nstd229human GRCh38 chr7: 30,282,953-30,283,056 , GRCh37.p13 chr7: 30,322,569-30,322,672 LOC105375218, ZNRF2
    nsv7040921inversion1nstd229human GRCh38 chr7: 29,656,957-32,757,617 , GRCh37.p13 chr7: 29,696,573-32,797,229 LSM5, RPS27P16, 51 more genes
    nsv6837194copy number variation1nstd229human GRCh38 chr7: 30,261,312-30,261,483 , GRCh37.p13 chr7: 30,300,928-30,301,099 LOC105375218
    nsv6836281copy number variation1nstd229human GRCh38 chr7: 30,269,175-30,272,054 , GRCh37.p13 chr7: 30,308,791-30,311,670 LOC105375218
    nsv6835730copy number variation1nstd229human GRCh38 chr7: 29,985,401-30,392,500 , GRCh37.p13 chr7: 30,025,017-30,432,116 PLEKHA8, FKBP14, 12 more genes
    nsv6835484copy number variation1nstd229human GRCh38 chr7: 30,241,107-30,245,616 , GRCh37.p13 chr7: 30,280,723-30,285,232 LOC105375218
    nsv6822777copy number variation1nstd229human GRCh38 chr7: 30,246,466-30,248,931 , GRCh37.p13 chr7: 30,286,082-30,288,547 LOC105375218
    nsv6822134copy number variation1nstd229human GRCh38 chr7: 30,257,538-30,263,308 , GRCh37.p13 chr7: 30,297,154-30,302,924 LOC105375218
    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
    nsv6612039copy number variation1nstd223human GRCh38 chr7: 30,269,634-30,270,135 , GRCh37.p13 chr7: 30,309,250-30,309,751 LOC105375218
    nsv6601669copy number variation1nstd223human GRCh38 chr7: 30,265,879-30,270,080 , GRCh37.p13 chr7: 30,305,495-30,309,696 LOC105375218
    nsv6570307inversion1nstd223human GRCh38 chr7: 30,169,322-32,154,185 , GRCh37.p13 chr7: 30,208,938-32,193,797 PDE1C, LOC105375217, 30 more genes
    nsv6556278inversion1nstd223human GRCh38 chr7: 29,684,558-32,729,318 , GRCh37.p13 chr7: 29,724,174-32,768,930 LOC105375219, CRHR2, 47 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
    nsv6312540copy number variation1nstd102humanUncertain significance GRCh37 chr7: 30,054,351-31,018,859 , GRCh38.p12 chr7: 30,014,735-30,979,244 GARS1-DT, GHRHR, 25 more genes
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