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Items: 1 to 20 of 172

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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
    nsv6830502copy number variation1nstd229human GRCh38 chr7: 99,486,765-99,489,390 , GRCh37.p13 chr7: 99,084,388-99,087,013 ZNF394, ZNF789
    nsv6829801copy number variation1nstd229human GRCh38 chr7: 99,474,883-99,486,226 , GRCh37.p13 chr7: 99,072,506-99,083,849 ZNF789, ZNF394
    nsv6829663copy number variation1nstd229human GRCh38 chr7: 99,496,144-99,496,193 , GRCh37.p13 chr7: 99,093,767-99,093,816 ZNF394
    nsv6824733copy number variation1nstd229human GRCh38 chr7: 99,488,849-99,491,293 , GRCh37.p13 chr7: 99,086,472-99,088,916 ZNF394
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6612375copy number variation1nstd223human GRCh38 chr7: 99,491,929-99,492,452 , GRCh37.p13 chr7: 99,089,552-99,090,075 ZNF394
    nsv6612178copy number variation1nstd223human GRCh38 chr7: 99,482,825-99,488,020 , GRCh37.p13 chr7: 99,080,448-99,085,643 ZNF789, ZNF394
    nsv6600962copy number variation1nstd223human GRCh38 chr7: 99,484,808-99,492,831 , GRCh37.p13 chr7: 99,082,431-99,090,454 ZNF789, ZNF394
    nsv6600855copy number variation1nstd223human GRCh38 chr7: 99,482,753-99,486,253 , GRCh37.p13 chr7: 99,080,376-99,083,876 ZNF394, ZNF789
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 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
    nsv6301255copy number variation1nstd186human GRCh37 chr7: 99,089,552-99,090,075 , GRCh38.p12 chr7: 99,491,929-99,492,452 ZNF394
    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
    nsv6135785copy number variation1nstd213human GRCh37 chr7: 76,690,000-99,250,001 , GRCh38.p12 chr7: 77,060,683-99,652,378 , ASNS, 283 more genes
    nsv6101547inversion1nstd212human GRCh38 chr7: 98,453,223-101,264,028 , GRCh37.p13 chr7: 98,082,535-100,907,309 , ACHE, 141 more genes
    nsv6013245copy number variation1nstd212human GRCh38 chr7: 99,490,239-99,490,300 , GRCh37.p13 chr7: 99,087,862-99,087,923 ZNF394
    nsv5926969copy number variation1nstd209human GRCh38 chr7: 99,482,780-99,486,242 , GRCh37.p13 chr7: 99,080,403-99,083,865 ZNF789, ZNF394
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