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Items: 1 to 20 of 221

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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
    nsv6837103copy number variation1nstd229human GRCh38 chr7: 99,420,893-99,430,493 , GRCh37.p13 chr7: 99,018,516-99,028,116 ATP5MF-PTCD1, PTCD1
    nsv6836522copy number variation1nstd229human GRCh38 chr7: 99,462,318-99,464,512 , GRCh37.p13 chr7: 99,059,941-99,062,135 ATP5MF-PTCD1, ATP5MF
    nsv6836311copy number variation1nstd229human GRCh38 chr7: 99,324,701-99,478,200 , GRCh37.p13 chr7: 98,922,324-99,075,823 ZNF789, PTCD1, 11 more genes
    nsv6832667copy number variation1nstd229human GRCh38 chr7: 99,425,437-99,431,776 , GRCh37.p13 chr7: 99,023,060-99,029,399 ATP5MF-PTCD1, PTCD1
    nsv6831358copy number variation1nstd229human GRCh38 chr7: 99,434,022-99,434,078 , GRCh37.p13 chr7: 99,031,645-99,031,701 ATP5MF-PTCD1, PTCD1
    nsv6830968copy number variation1nstd229human GRCh38 chr7: 99,426,295-99,451,798 , GRCh37.p13 chr7: 99,023,918-99,049,421 LOC100131859, ATP5MF-PTCD1, 2 more genes
    nsv6828702copy number variation1nstd229human GRCh38 chr7: 99,411,578-99,417,849 , GRCh37.p13 chr7: 99,009,201-99,015,472 BUD31, ATP5MF-PTCD1, 1 more genes
    nsv6824377copy number variation1nstd229human GRCh38 chr7: 99,353,075-99,430,260 , GRCh37.p13 chr7: 98,950,698-99,027,883 MIR12119, PTCD1, 5 more genes
    nsv6821938copy number variation1nstd229human GRCh38 chr7: 99,422,494-99,430,146 , GRCh37.p13 chr7: 99,020,117-99,027,769 ATP5MF-PTCD1, PTCD1
    nsv6821329copy number variation1nstd229human GRCh38 chr7: 99,213,401-99,478,200 , GRCh37.p13 chr7: 98,811,024-99,075,823 MIR12119, KPNA7, 13 more genes
    nsv6818125copy number variation1nstd229human GRCh38 chr7: 99,414,655-99,418,027 , GRCh37.p13 chr7: 99,012,278-99,015,650 ATP5MF-PTCD1, BUD31, 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
    nsv6616732copy number variation1nstd223human GRCh38 chr7: 99,419,758-99,420,265 , GRCh37.p13 chr7: 99,017,381-99,017,888 ATP5MF-PTCD1, PTCD1, 1 more genes
    nsv6614379copy number variation1nstd223human GRCh38 chr7: 99,434,021-99,434,078 , GRCh37.p13 chr7: 99,031,644-99,031,701 ATP5MF-PTCD1, PTCD1
    nsv6613451copy number variation1nstd223human GRCh38 chr7: 99,411,958-99,414,850 , GRCh37.p13 chr7: 99,009,581-99,012,473 PTCD1, ATP5MF-PTCD1, 1 more genes
    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
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