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Items: 1 to 20 of 103

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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
    nsv7040921inversion1nstd229human GRCh38 chr7: 29,656,957-32,757,617 , GRCh37.p13 chr7: 29,696,573-32,797,229 LSM5, RPS27P16, 51 more genes
    nsv6825478copy number variation1nstd229human GRCh38 chr7: 31,333,701-31,342,300 , GRCh37.p13 chr7: 31,373,315-31,381,914 NEUROD6
    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
    nsv6820400copy number variation1nstd229human GRCh38 chr7: 31,303,221-31,336,141 , GRCh37.p13 chr7: 31,342,835-31,375,755 NEUROD6
    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
    nsv6617866copy number variation1nstd223human GRCh38 chr7: 31,335,901-31,337,200 , GRCh37.p13 chr7: 31,375,515-31,376,814 NEUROD6
    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
    nsv6136176copy number variation1nstd213human GRCh37 chr7: 30,790,000-31,570,001 , GRCh38.p12 chr7: 30,750,384-31,530,387 MINDY4, ITPRID1, 13 more genes
    nsv5919512copy number variation1nstd209human GRCh38 chr7: 26,509,679-33,120,288 , GRCh37.p13 chr7: 26,549,298-33,159,900 , CPVL-AS1, 126 more genes
    nsv5914132copy number variation1nstd209human GRCh38 chr7: 26,936,027-36,716,695 , GRCh37.p13 chr7: 26,975,646-36,756,300 , HOXA7, 162 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
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