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Items: 1 to 20 of 135

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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
    nsv7042397inversion1nstd229human GRCh38 chr7: 30,756,363-30,797,967 , GRCh37.p13 chr7: 30,795,979-30,837,583 INMT, INMT-MINDY4, 1 more genes
    nsv7040921inversion1nstd229human GRCh38 chr7: 29,656,957-32,757,617 , GRCh37.p13 chr7: 29,696,573-32,797,229 LSM5, RPS27P16, 51 more genes
    nsv7039111inversion1nstd229human GRCh38 chr7: 30,750,541-30,770,693 , GRCh37.p13 chr7: 30,790,157-30,810,309 INMT, INMT-MINDY4, 2 more genes
    nsv6834072copy number variation1nstd229human GRCh38 chr7: 30,612,963-31,127,528 , GRCh37.p13 chr7: 30,652,579-31,167,142 CRHR2, GHRHR, 11 more genes
    nsv6826739copy number variation1nstd229human GRCh38 chr7: 30,702,848-31,260,094 , GRCh37.p13 chr7: 30,742,464-31,299,708 OSBPL9P6, LOC105375219, 11 more genes
    nsv6826442copy number variation1nstd229human GRCh38 chr7: 30,752,942-30,753,744 , GRCh37.p13 chr7: 30,792,558-30,793,360 INMT, INMT-MINDY4
    nsv6824831copy number variation1nstd229human GRCh38 chr7: 30,756,201-30,776,300 , GRCh37.p13 chr7: 30,795,817-30,815,916 INMT, INMT-MINDY4, 1 more genes
    nsv6821205copy number variation1nstd229human GRCh38 chr7: 30,523,146-31,374,858 , GRCh37.p13 chr7: 30,562,762-31,414,472 LOC107986781, LOC105375220, 16 more genes
    nsv6637041copy number variation1nstd102humanUncertain significance GRCh37 chr7: 30,567,050-31,415,774 , GRCh38.p12 chr7: 30,527,434-31,376,160 GARS1, CRHR2, 16 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
    nsv6616451copy number variation1nstd223human GRCh38 chr7: 30,612,963-31,127,528 , GRCh37.p13 chr7: 30,652,579-31,167,142 LOC105375220, AQP1, 11 more genes
    nsv6602744copy number variation1nstd223human GRCh38 chr7: 30,757,299-30,759,138 , GRCh37.p13 chr7: 30,796,915-30,798,754 INMT, INMT-MINDY4
    nsv6571204inversion1nstd223human GRCh38 chr7: 30,750,535-30,770,694 , GRCh37.p13 chr7: 30,790,151-30,810,310 INMT, MINDY4, 2 more genes
    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
    nsv6314821copy number variation1nstd102humanUncertain significance GRCh37 chr7: 30,655,492-31,018,859 , GRCh38.p12 chr7: 30,615,876-30,979,244 GARS1, LOC105375219, 8 more genes
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