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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144799insertion1nstd232human GRCh37.p13 chr9: 71,827,887-71,827,887 , GRCh38.p12 chr9: 69,212,971-69,212,971 TJP2
    nsv7093070copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,836,411-71,837,142 , GRCh38 chr9: 69,221,495-69,222,226 TJP2
    nsv7069024inversion1nstd229human GRCh38 chr9: 69,226,041-69,229,109 , GRCh37.p13 chr9: 71,840,957-71,844,025 TJP2
    nsv7059369inversion1nstd229human GRCh38 chr9: 69,068,268-69,425,843 , GRCh37.p13 chr9: 71,683,184-72,040,759 TJP2, BANCR, 3 more genes
    nsv6877761copy number variation1nstd229human GRCh38 chr9: 69,218,675-69,245,452 , GRCh37.p13 chr9: 71,833,591-71,860,368 TJP2
    nsv6877449copy number variation1nstd229human GRCh38 chr9: 69,223,049-69,223,087 , GRCh37.p13 chr9: 71,837,965-71,838,003 TJP2
    nsv6877358copy number variation1nstd229human GRCh38 chr9: 69,151,213-69,226,603 , GRCh37.p13 chr9: 71,766,129-71,841,519 TJP2
    nsv6877153copy number variation1nstd229human GRCh38 chr9: 69,163,025-69,163,328 , GRCh37.p13 chr9: 71,777,941-71,778,244 TJP2
    nsv6876908copy number variation1nstd229human GRCh38 chr9: 68,843,470-69,163,021 , GRCh37.p13 chr9: 71,458,386-71,777,937 PRKACG, LOC101927069, 4 more genes
    nsv6876369copy number variation1nstd229human GRCh38 chr9: 68,982,687-69,234,459 , GRCh37.p13 chr9: 71,597,603-71,849,375 PRKACG, FXN, 2 more genes
    nsv6874868copy number variation1nstd229human GRCh38 chr9: 69,221,115-69,221,164 , GRCh37.p13 chr9: 71,836,031-71,836,080 TJP2
    nsv6872776copy number variation1nstd229human GRCh38 chr9: 69,116,585-69,124,488 , GRCh37.p13 chr9: 71,731,501-71,739,404 TJP2
    nsv6871735copy number variation1nstd229human GRCh38 chr9: 69,123,206-69,128,441 , GRCh37.p13 chr9: 71,738,122-71,743,357 TJP2
    nsv6870645copy number variation1nstd229human GRCh38 chr9: 69,232,258-69,656,226 , GRCh37.p13 chr9: 71,847,174-72,271,142 BANCR, ENTREP1, 2 more genes
    nsv6870496copy number variation1nstd229human GRCh38 chr9: 68,797,815-69,382,643 , GRCh37.p13 chr9: 71,412,731-71,997,559 BANCR, PIP5K1B, 6 more genes
    nsv6870132copy number variation1nstd229human GRCh38 chr9: 69,182,226-69,195,539 , GRCh37.p13 chr9: 71,797,142-71,810,455 TJP2
    nsv6868280copy number variation1nstd229human GRCh38 chr9: 69,175,279-69,175,576 , GRCh37.p13 chr9: 71,790,195-71,790,492 TJP2
    nsv6868263copy number variation1nstd229human GRCh38 chr9: 68,912,830-69,375,668 , GRCh37.p13 chr9: 71,527,746-71,990,584 PRKACG, LOC101927069, 6 more genes
    nsv6868101copy number variation1nstd229human GRCh38 chr9: 69,189,611-69,190,086 , GRCh37.p13 chr9: 71,804,527-71,805,002 TJP2
    nsv6866525copy number variation1nstd229human GRCh38 chr9: 68,550,745-69,178,058 , GRCh37.p13 chr9: 71,165,661-71,792,974 PABIR1, LOC105376071, 9 more genes
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