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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7064071inversion1nstd229human GRCh38 chr9: 114,393,214-114,752,294 , GRCh37.p13 chr9: 117,155,494-117,514,574 TMEM268, LOC107987121, 8 more genes
    nsv6877074copy number variation1nstd229human GRCh38 chr9: 114,443,799-114,451,713 , GRCh37.p13 chr9: 117,206,079-117,213,993 WHRN
    nsv6873571copy number variation1nstd229human GRCh38 chr9: 114,442,228-114,455,441 , GRCh37.p13 chr9: 117,204,508-117,217,721 WHRN
    nsv6873224copy number variation1nstd229human GRCh38 chr9: 114,429,312-114,429,477 , GRCh37.p13 chr9: 117,191,592-117,191,757 WHRN
    nsv6870069copy number variation1nstd229human GRCh38 chr9: 114,479,753-114,532,254 , GRCh37.p13 chr9: 117,242,033-117,294,534 WHRN, LOC100131877
    nsv6869905copy number variation1nstd229human GRCh38 chr9: 114,476,881-114,477,224 , GRCh37.p13 chr9: 117,239,161-117,239,504 WHRN
    nsv6867932copy number variation1nstd229human GRCh38 chr9: 114,484,531-114,487,237 , GRCh37.p13 chr9: 117,246,811-117,249,517 WHRN
    nsv6867538copy number variation1nstd229human GRCh38 chr9: 114,457,568-114,466,476 , GRCh37.p13 chr9: 117,219,848-117,228,756 WHRN
    nsv6862878copy number variation1nstd229human GRCh38 chr9: 114,413,440-114,443,834 , GRCh37.p13 chr9: 117,175,720-117,206,114 WHRN
    nsv6862869copy number variation1nstd229human GRCh38 chr9: 113,935,701-114,504,800 , GRCh37.p13 chr9: 116,697,981-117,267,080 COL27A1, LOC107987120, 11 more genes
    nsv6862364copy number variation1nstd229human GRCh38 chr9: 114,416,590-114,421,434 , GRCh37.p13 chr9: 117,178,870-117,183,714 WHRN
    nsv6860304copy number variation1nstd229human GRCh38 chr9: 114,283,749-115,033,639 , GRCh37.p13 chr9: 117,046,029-117,795,918 COL27A1, TMEM268, 16 more genes
    nsv6859557copy number variation1nstd229human GRCh38 chr9: 114,434,171-114,434,242 , GRCh37.p13 chr9: 117,196,451-117,196,522 WHRN
    nsv6859029copy number variation1nstd229human GRCh38 chr9: 114,468,844-114,475,722 , GRCh37.p13 chr9: 117,231,124-117,238,002 WHRN
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633395copy number variation3nstd224human GRCh37 chr9: 116,958,266-117,453,668 , GRCh38.p12 chr9: 114,195,986-114,691,388 ORM2, AKNA, 12 more genes
    nsv6633116copy number variation1nstd224human GRCh37 chr9: 116,952,274-117,453,668 , GRCh38.p12 chr9: 114,189,994-114,691,388 ORM1, WHRN, 12 more genes
    nsv6572854inversion1nstd223human GRCh38 chr9: 114,422,475-114,422,589 , GRCh37.p13 chr9: 117,184,755-117,184,869 WHRN
    nsv6454716copy number variation1nstd223human GRCh38 chr9: 114,416,588-114,421,433 , GRCh37.p13 chr9: 117,178,868-117,183,713 WHRN
    nsv6452122copy number variation1nstd223human GRCh38 chr9: 114,150,401-114,423,800 , GRCh37.p13 chr9: 116,912,681-117,186,080 MIR455, ORM2, 6 more genes
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