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Items: 1 to 20 of 733

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147454copy number variation1nstd232human GRCh37.p13 chr20: 34,438,498-34,438,548 , GRCh38.p12 chr20: 35,850,576-35,850,626 PHF20, COX7BP2
    nsv7037266copy number variation1nstd229human GRCh38 chr20: 35,948,949-35,949,528 , GRCh37.p13 chr20: 34,536,871-34,537,450 PHF20
    nsv7036332copy number variation1nstd229human GRCh38 chr20: 35,850,591-35,850,627 , GRCh37.p13 chr20: 34,438,513-34,438,549 PHF20, COX7BP2
    nsv7035875copy number variation1nstd229human GRCh38 chr20: 35,882,914-35,888,692 , GRCh37.p13 chr20: 34,470,836-34,476,614 RNU4-40P, PHF20
    nsv7035673copy number variation1nstd229human GRCh38 chr20: 35,786,201-35,793,500 , GRCh37.p13 chr20: 34,374,123-34,381,422 PHF20
    nsv7035354copy number variation1nstd229human GRCh38 chr20: 35,812,696-35,812,792 , GRCh37.p13 chr20: 34,400,618-34,400,714 PHF20
    nsv7032811copy number variation1nstd229human GRCh38 chr20: 35,910,301-35,913,900 , GRCh37.p13 chr20: 34,498,223-34,501,822 PHF20
    nsv7030496copy number variation1nstd229human GRCh38 chr20: 35,791,147-35,792,480 , GRCh37.p13 chr20: 34,379,069-34,380,402 PHF20
    nsv7030097copy number variation1nstd229human GRCh38 chr20: 35,869,914-35,870,059 , GRCh37.p13 chr20: 34,457,836-34,457,981 PHF20
    nsv7029777copy number variation1nstd229human GRCh38 chr20: 35,890,894-35,893,567 , GRCh37.p13 chr20: 34,478,816-34,481,489 PHF20
    nsv7029400copy number variation1nstd229human GRCh38 chr20: 35,815,342-35,816,871 , GRCh37.p13 chr20: 34,403,264-34,404,793 PHF20
    nsv7026954copy number variation1nstd229human GRCh38 chr20: 35,848,032-35,855,407 , GRCh37.p13 chr20: 34,435,954-34,443,329 PHF20, COX7BP2
    nsv7024726copy number variation1nstd229human GRCh38 chr20: 35,848,291-35,853,814 , GRCh37.p13 chr20: 34,436,213-34,441,736 COX7BP2, PHF20
    nsv7024308copy number variation1nstd229human GRCh38 chr20: 35,809,977-35,810,473 , GRCh37.p13 chr20: 34,397,899-34,398,395 PHF20
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv7021149copy number variation1nstd229human GRCh38 chr20: 35,900,424-35,904,181 , GRCh37.p13 chr20: 34,488,346-34,492,103 PHF20
    nsv7020699copy number variation1nstd229human GRCh38 chr20: 35,889,180-35,890,204 , GRCh37.p13 chr20: 34,477,102-34,478,126 PHF20
    nsv7020369copy number variation1nstd229human GRCh38 chr20: 35,777,869-35,780,278 , GRCh37.p13 chr20: 34,365,791-34,368,200 PHF20
    nsv7020202copy number variation1nstd229human GRCh38 chr20: 35,803,377-35,805,437 , GRCh37.p13 chr20: 34,391,299-34,393,359 PHF20
    nsv7019999copy number variation1nstd229human GRCh38 chr20: 35,486,342-36,114,422 , GRCh37.p13 chr20: 34,074,168-34,702,344 HMGB3P2, NFS1, 24 more genes
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