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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051143inversion1nstd229human GRCh38 chr7: 30,380,083-32,474,134 , GRCh37.p13 chr7: 30,419,699-32,513,746 GHRHR, NOD1, 26 more genes
    nsv7046140inversion1nstd229human GRCh38 chr7: 30,431,026-30,629,349 , GRCh37.p13 chr7: 30,470,642-30,668,965 GARS1, LOC100287825, 3 more genes
    nsv7041657inversion1nstd229human GRCh38 chr7: 30,430,744-30,437,706 , GRCh37.p13 chr7: 30,470,360-30,477,322 NOD1
    nsv7040921inversion1nstd229human GRCh38 chr7: 29,656,957-32,757,617 , GRCh37.p13 chr7: 29,696,573-32,797,229 LSM5, RPS27P16, 51 more genes
    nsv6836564copy number variation1nstd229human GRCh38 chr7: 30,428,068-30,428,125 , GRCh37.p13 chr7: 30,467,684-30,467,741 NOD1
    nsv6835863copy number variation1nstd229human GRCh38 chr7: 30,434,932-30,435,005 , GRCh37.p13 chr7: 30,474,548-30,474,621 NOD1
    nsv6834897copy number variation1nstd229human GRCh38 chr7: 30,462,171-30,462,942 , GRCh37.p13 chr7: 30,501,787-30,502,558 NOD1
    nsv6834776copy number variation1nstd229human GRCh38 chr7: 30,476,708-30,480,673 , GRCh37.p13 chr7: 30,516,324-30,520,289 NOD1
    nsv6832108copy number variation1nstd229human GRCh38 chr7: 30,469,700-30,471,069 , GRCh37.p13 chr7: 30,509,316-30,510,685 NOD1
    nsv6830096copy number variation1nstd229human GRCh38 chr7: 30,447,560-30,450,794 , GRCh37.p13 chr7: 30,487,176-30,490,410 NOD1
    nsv6822613copy number variation1nstd229human GRCh38 chr7: 30,425,556-30,430,507 , GRCh37.p13 chr7: 30,465,172-30,470,123 NOD1
    nsv6821138copy number variation1nstd229human GRCh38 chr7: 30,463,200-30,465,690 , GRCh37.p13 chr7: 30,502,816-30,505,306 NOD1
    nsv6819201copy number variation1nstd229human GRCh38 chr7: 30,398,316-30,514,280 , GRCh37.p13 chr7: 30,437,932-30,553,896 NOD1, GGCT, 1 more genes
    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
    nsv6613712copy number variation1nstd223human GRCh38 chr7: 30,425,556-30,430,502 , GRCh37.p13 chr7: 30,465,172-30,470,118 NOD1
    nsv6602725copy number variation1nstd223human GRCh38 chr7: 30,463,200-30,465,690 , GRCh37.p13 chr7: 30,502,816-30,505,306 NOD1
    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
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