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Items: 1 to 20 of 173

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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
    nsv6829395copy number variation1nstd229human GRCh38 chr7: 100,076,358-100,093,492 , GRCh37.p13 chr7: 99,673,981-99,691,115 MIR25, COPS6, 4 more genes
    nsv6818846copy number variation1nstd229human GRCh38 chr7: 100,066,392-100,069,369 , GRCh37.p13 chr7: 99,664,015-99,666,992 ZNF3
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6614776copy number variation1nstd223human GRCh38 chr7: 99,943,801-101,566,300 , GRCh37.p13 chr7: 99,541,424-101,209,580 MUC12, FBXO24, 95 more genes
    nsv6611745copy number variation1nstd223human GRCh38 chr7: 100,066,410-100,069,349 , GRCh37.p13 chr7: 99,664,033-99,666,972 ZNF3
    nsv6611024copy number variation1nstd223human GRCh38 chr7: 100,068,331-100,069,079 , GRCh37.p13 chr7: 99,665,954-99,666,702 ZNF3
    nsv6601568copy number variation1nstd223human GRCh38 chr7: 100,078,427-100,082,517 , GRCh37.p13 chr7: 99,676,050-99,680,140 ZNF3
    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
    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
    nsv6239503mobile element insertion1nstd215human GRCh38 chr7: 100,076,147-100,076,147 , GRCh37.p13 chr7: 99,673,770-99,673,770 ZNF3
    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
    nsv5979182inversion1nstd209human GRCh38 chr7: 99,981,419-101,289,122 , GRCh37.p13 chr7: 99,579,042-100,932,403 , ACHE, 92 more genes
    nsv5959083insertion1nstd209human GRCh38 chr7: 100,076,130-100,076,130 , GRCh37.p13 chr7: 99,673,753-99,673,753 ZNF3
    nsv5956121insertion1nstd209human GRCh38 chr7: 100,067,020-100,067,020 , GRCh37.p13 chr7: 99,664,643-99,664,643 ZNF3
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