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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122791copy number variation1nstd186human GRCh37 chr9: 135,401,937-135,404,910 , GRCh38.p12 chr9: 132,526,550-132,529,523 CFAP77
    nsv5961951insertion1nstd209human GRCh38 chr9: 132,519,499-132,519,499 , GRCh37.p13 chr9: 135,394,886-135,394,886 CFAP77
    nsv5954864insertion1nstd209human GRCh38 chr9: 132,559,346-132,559,346 , GRCh37.p13 chr9: 135,434,733-135,434,733 CFAP77
    nsv5948729insertion1nstd209human GRCh38 chr9: 132,486,025-132,486,025 , GRCh37.p13 chr9: 135,361,412-135,361,412 CFAP77
    nsv5926086copy number variation1nstd209human GRCh38 chr9: 132,421,610-132,421,685 , GRCh37.p13 chr9: 135,296,997-135,297,072 RNU5D-2P, CFAP77
    nsv5924724copy number variation1nstd209human GRCh38 chr9: 132,514,046-132,514,128 , GRCh37.p13 chr9: 135,389,433-135,389,515 CFAP77
    nsv5923958copy number variation1nstd209human GRCh38 chr9: 132,541,472-132,541,661 , GRCh37.p13 chr9: 135,416,859-135,417,048 CFAP77
    nsv5922853copy number variation1nstd209human GRCh38 chr9: 132,524,781-132,525,151 , GRCh37.p13 chr9: 135,400,168-135,400,538 CFAP77
    nsv5921816copy number variation1nstd209human GRCh38 chr9: 132,513,903-132,514,112 , GRCh37.p13 chr9: 135,389,290-135,389,499 CFAP77
    nsv5920017copy number variation1nstd209human GRCh38 chr9: 132,453,310-132,453,428 , GRCh37.p13 chr9: 135,328,697-135,328,815 CFAP77
    nsv5918480copy number variation1nstd209human GRCh38 chr9: 132,438,938-132,443,315 , GRCh37.p13 chr9: 135,314,325-135,318,702 CFAP77
    nsv5918254copy number variation1nstd209human GRCh38 chr9: 132,526,542-132,529,522 , GRCh37.p13 chr9: 135,401,929-135,404,909 CFAP77
    nsv5864677copy number variation1nstd209human GRCh38 chr9: 132,559,766-132,570,718 , GRCh37.p13 chr9: 135,435,153-135,446,105 CFAP77
    nsv5852409copy number variation1nstd209human GRCh38 chr9: 132,562,606-132,567,105 , GRCh37.p13 chr9: 135,437,993-135,442,492 CFAP77
    nsv5852109copy number variation2nstd209human GRCh38 chr9: 132,440,954-132,442,053 , GRCh37.p13 chr9: 135,316,341-135,317,440 CFAP77
    nsv5851129copy number variation1nstd209human GRCh38 chr9: 132,440,754-132,443,553 , GRCh37.p13 chr9: 135,316,141-135,318,940 CFAP77
    nsv5850955copy number variation1nstd209human GRCh38 chr9: 132,564,506-132,570,706 , GRCh37.p13 chr9: 135,439,893-135,446,093 CFAP77
    nsv5639171insertion1nstd207human GRCh38 chr9: 132,519,499-132,519,499 , GRCh37.p13 chr9: 135,394,886-135,394,886 CFAP77
    nsv5603244copy number variation1nstd207human GRCh38 chr9: 132,524,781-132,525,151 , GRCh37.p13 chr9: 135,400,168-135,400,538 CFAP77
    nsv5601866copy number variation1nstd207human GRCh38 chr9: 132,421,610-132,421,685 , GRCh37.p13 chr9: 135,296,997-135,297,072 CFAP77, RNU5D-2P
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