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Items: 1 to 20 of 206

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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
    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
    nsv6824195copy number variation1nstd229human GRCh38 chr7: 99,355,133-99,356,874 , GRCh37.p13 chr7: 98,952,756-98,954,497 ARPC1A
    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
    nsv6609908copy number variation1nstd223human GRCh38 chr7: 99,341,202-99,343,359 , GRCh37.p13 chr7: 98,938,825-98,940,982 ARPC1A
    nsv6604003copy number variation1nstd223human GRCh38 chr7: 99,354,251-99,356,333 , GRCh37.p13 chr7: 98,951,874-98,953,956 ARPC1A
    nsv6600351copy number variation1nstd223human GRCh38 chr7: 99,356,242-99,356,776 , GRCh37.p13 chr7: 98,953,865-98,954,399 ARPC1A
    nsv6562600inversion1nstd223human GRCh38 chr7: 99,342,415-99,342,729 , GRCh37.p13 chr7: 98,940,038-98,940,352 ARPC1A
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 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
    nsv6073283insertion1nstd212human GRCh38 chr7: 99,360,786-99,360,786 , GRCh37.p13 chr7: 98,958,409-98,958,409 ARPC1A
    nsv6067278insertion1nstd212human GRCh38 chr7: 99,363,847-99,363,847 , GRCh37.p13 chr7: 98,961,470-98,961,470 ARPC1A
    nsv5915732copy number variation1nstd209human GRCh38 chr7: 99,219,897-99,375,922 , GRCh37.p13 chr7: 98,817,520-98,973,545 ARPC1B, ARPC1A, 3 more genes
    nsv5718350mobile element insertion1nstd211human GRCh38 chr7: 99,359,851-99,359,851 , GRCh37.p13 chr7: 98,957,474-98,957,474 ARPC1A

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