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Items: 1 to 20 of 166

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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
    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
    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
    nsv6619102copy number variation1nstd223human GRCh38 chr7: 99,472,612-99,481,757 , GRCh37.p13 chr7: 99,070,235-99,079,380 ZNF789
    nsv6612178copy number variation1nstd223human GRCh38 chr7: 99,482,825-99,488,020 , GRCh37.p13 chr7: 99,080,448-99,085,643 ZNF789, ZNF394
    nsv6610661copy number variation1nstd223human GRCh38 chr7: 99,482,201-99,483,800 , GRCh37.p13 chr7: 99,079,824-99,081,423 ZNF789
    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
    nsv6569381inversion1nstd223human GRCh38 chr7: 99,481,530-99,482,866 , GRCh37.p13 chr7: 99,079,153-99,080,489 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
    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
    nsv6016954copy number variation1nstd212human GRCh38 chr7: 99,472,567-99,472,943 , GRCh37.p13 chr7: 99,070,190-99,070,566 ZNF789
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