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Items: 1 to 20 of 99

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7040921inversion1nstd229human GRCh38 chr7: 29,656,957-32,757,617 , GRCh37.p13 chr7: 29,696,573-32,797,229 LSM5, RPS27P16, 51 more genes
    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
    nsv6819039copy number variation1nstd229human GRCh38 chr7: 30,336,832-30,397,423 , GRCh37.p13 chr7: 30,376,448-30,437,039 LINC01176, DKFZP586I1420, 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
    nsv6600806copy number variation1nstd223human GRCh38 chr7: 30,369,630-30,370,200 , GRCh37.p13 chr7: 30,409,246-30,409,816 DKFZP586I1420
    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
    nsv6136988copy number variation1nstd213human GRCh37 chr7: 30,070,000-30,740,001 , GRCh38.p12 chr7: 30,030,384-30,700,385 CRHR2, NOD1, 16 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
    nsv5231937copy number variation1nstd204human GRCh38.p13 chr7: 30,366,601-30,368,900 , GRCh37.p13 chr7: 30,406,217-30,408,516 ZNRF2, DKFZP586I1420
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4953549copy number variation1nstd200human GRCh38 chr7: 30,336,832-30,397,423 , GRCh37.p13 chr7: 30,376,448-30,437,039 DKFZP586I1420, ZNRF2, 1 more genes
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