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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148181copy number variation1nstd102humanPathogenic GRCh38 chr7: 98,454,022-100,723,798 , GRCh37.p13 chr7: 98,083,334-100,321,421 LAMTOR4, PTCD1, 107 more genes
    nsv7098147copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,507,659-100,860,555 , GRCh38.p12 chr7: 98,910,036-101,217,274 SLC12A9, LOC105375423, 127 more genes
    nsv7052776inversion1nstd229human GRCh38 chr7: 96,709,838-100,726,550 , GRCh37.p13 chr7: 96,339,150-100,324,173 TMEM225B, PILRB, 141 more genes
    nsv7041352inversion1nstd229human GRCh38 chr7: 99,892,476-99,892,500 , GRCh37.p13 chr7: 99,490,099-99,490,123 TRIM4
    nsv7040152inversion1nstd229human GRCh38 chr7: 99,908,501-99,922,340 , GRCh37.p13 chr7: 99,506,124-99,519,963 TRIM4, LOC101927610, 1 more genes
    nsv6828543copy number variation1nstd229human GRCh38 chr7: 99,919,542-99,926,240 , GRCh37.p13 chr7: 99,517,165-99,523,863 TRIM4, LOC101927610, 1 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
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313503copy number variation1nstd102humanPathogenic GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253 GJC3, LAMB4, 237 more genes
    nsv6312372copy number variation1nstd102humanPathogenic GRCh37 chr7: 98,983,338-100,860,555 , GRCh38.p12 chr7: 99,385,715-101,217,274 AZGP1P1, MOGAT3, 119 more genes
    nsv6302366copy number variation1nstd186human GRCh37 chr7: 99,515,212-99,516,100 , GRCh38.p12 chr7: 99,917,589-99,918,477 TRIM4, LOC101927610
    nsv6290864copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,755,291-99,886,571 , GRCh38.p12 chr7: 99,157,668-100,288,948 LAMTOR4, OR2AE1, 62 more genes
    nsv6136217copy number variation1nstd213human GRCh37 chr7: 99,390,000-104,070,001 , GRCh38.p12 chr7: 99,792,377-104,429,553 AZGP1, CRYZP1, 157 more genes
    nsv6101547inversion1nstd212human GRCh38 chr7: 98,453,223-101,264,028 , GRCh37.p13 chr7: 98,082,535-100,907,309 , ACHE, 141 more genes
    nsv5907841copy number variation1nstd209human GRCh38 chr7: 99,896,459-99,899,337 , GRCh37.p13 chr7: 99,494,082-99,496,960 TRIM4
    nsv5562394sequence alteration1nstd206human GRCh38 chr7: 99,913,224-99,940,026 , GRCh37.p13 chr7: 99,510,847-99,537,649 TRIM4, GJC3, 1 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
    nsv5490601copy number variation1nstd206human GRCh38 chr7: 99,917,589-99,918,477 , GRCh37.p13 chr7: 99,515,212-99,516,100 LOC101927610, TRIM4
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
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