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Items: 1 to 20 of 128

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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
    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
    nsv6834311copy number variation1nstd229human GRCh38 chr7: 99,393,908-99,398,442 , GRCh37.p13 chr7: 98,991,531-98,996,065 PDAP1, ARPC1B
    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
    nsv6821481copy number variation1nstd229human GRCh38 chr7: 99,395,301-99,397,300 , GRCh37.p13 chr7: 98,992,924-98,994,923 ARPC1B, PDAP1
    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
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6600523copy number variation1nstd223human GRCh38 chr7: 99,405,391-99,410,400 , GRCh37.p13 chr7: 99,003,014-99,008,023 PDAP1, MIR12119, 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
    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
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    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
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 more genes
    nsv5215180mobile element deletion1nstd204human GRCh38.p13 chr7: 99,405,330-99,405,688 , GRCh37.p13 chr7: 99,002,953-99,003,311 PDAP1
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