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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129544insertion1nstd186human GRCh37 chr17: 80,080,352-80,080,359 , GRCh38.p12 chr17: 82,122,476-82,122,483 CCDC57
    nsv6127785copy number variation1nstd186human GRCh37 chr17: 80,080,286-80,080,385 , GRCh38.p12 chr17: 82,122,410-82,122,509 CCDC57
    nsv5978296inversion1nstd209human GRCh38 chr17: 81,945,255-82,544,213 , GRCh37.p13 chr17: 79,903,131-80,502,089 , CD7, 29 more genes
    nsv5973267inversion1nstd209human GRCh38 chr17: 82,157,630-82,194,004 , GRCh37.p13 chr17: 80,115,506-80,151,880 CCDC57
    nsv5970311insertion1nstd209human GRCh38 chr17: 82,122,432-82,122,432 , GRCh37.p13 chr17: 80,080,308-80,080,308 CCDC57
    nsv5947227copy number variation1nstd209human GRCh38 chr17: 82,151,052-82,151,429 , GRCh37.p13 chr17: 80,108,928-80,109,305 CCDC57
    nsv5944325copy number variation1nstd209human GRCh38 chr17: 82,150,028-82,150,369 , GRCh37.p13 chr17: 80,107,904-80,108,245 CCDC57
    nsv5944170copy number variation1nstd209human GRCh38 chr17: 82,187,537-82,187,751 , GRCh37.p13 chr17: 80,145,413-80,145,627 CCDC57
    nsv5940548copy number variation1nstd209human GRCh38 chr17: 82,148,587-82,149,106 , GRCh37.p13 chr17: 80,106,463-80,106,982 CCDC57
    nsv5938055copy number variation1nstd209human GRCh38 chr17: 82,160,327-82,160,378 , GRCh37.p13 chr17: 80,118,203-80,118,254 CCDC57
    nsv5934496copy number variation1nstd209human GRCh38 chr17: 82,198,719-82,199,205 , GRCh37.p13 chr17: 80,156,595-80,157,081 CCDC57
    nsv5933227copy number variation1nstd209human GRCh38 chr17: 82,148,368-82,148,439 , GRCh37.p13 chr17: 80,106,244-80,106,315 CCDC57
    nsv5932780copy number variation1nstd209human GRCh38 chr17: 82,151,250-82,151,357 , GRCh37.p13 chr17: 80,109,126-80,109,233 CCDC57
    nsv5931334copy number variation1nstd209human GRCh38 chr17: 82,154,555-82,154,845 , GRCh37.p13 chr17: 80,112,431-80,112,721 CCDC57
    nsv5928347copy number variation1nstd209human GRCh38 chr17: 82,148,246-82,149,082 , GRCh37.p13 chr17: 80,106,122-80,106,958 CCDC57
    nsv5885342copy number variation1nstd209human GRCh38 chr17: 82,145,119-82,163,777 , GRCh37.p13 chr17: 80,102,995-80,121,653 CCDC57
    nsv5879491copy number variation1nstd209human GRCh38 chr17: 82,126,399-82,144,493 , GRCh37.p13 chr17: 80,084,275-80,102,369 CCDC57
    nsv5876253copy number variation1nstd209human GRCh38 chr17: 82,087,067-82,102,339 , GRCh37.p13 chr17: 80,044,943-80,060,215 FASN, SNORD134, 1 more genes
    nsv5870383copy number variation1nstd209human GRCh38 chr17: 82,167,978-82,178,965 , GRCh37.p13 chr17: 80,125,854-80,136,841 CCDC57
    nsv5729065mobile element insertion1nstd211human GRCh38 chr17: 82,142,027-82,142,027 , GRCh37.p13 chr17: 80,099,903-80,099,903 CCDC57
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