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Items: 1 to 20 of 1398

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962056insertion1nstd209human GRCh38 chr9: 16,682,301-16,682,301 , GRCh37.p13 chr9: 16,682,299-16,682,299 BNC2
    nsv5960861insertion1nstd209human GRCh38 chr9: 16,451,512-16,451,512 , GRCh37.p13 chr9: 16,451,510-16,451,510 BNC2
    nsv5925845copy number variation1nstd209human GRCh38 chr9: 16,482,072-16,482,283 , GRCh37.p13 chr9: 16,482,070-16,482,281 BNC2
    nsv5916747copy number variation1nstd209human GRCh38 chr9: 16,463,288-16,463,594 , GRCh37.p13 chr9: 16,463,286-16,463,592 BNC2
    nsv5916196copy number variation1nstd209human GRCh38 chr9: 16,858,589-16,859,864 , GRCh37.p13 chr9: 16,858,587-16,859,862 BNC2
    nsv5916136copy number variation1nstd209human GRCh38 chr9: 16,502,915-16,504,532 , GRCh37.p13 chr9: 16,502,913-16,504,530 BNC2
    nsv5908155copy number variation1nstd209human GRCh38 chr9: 16,498,107-16,498,202 , GRCh37.p13 chr9: 16,498,105-16,498,200 BNC2
    nsv5907800copy number variation1nstd209human GRCh38 chr9: 16,461,567-16,468,846 , GRCh37.p13 chr9: 16,461,565-16,468,844 BNC2
    nsv5907794copy number variation1nstd209human GRCh38 chr9: 16,421,497-16,426,144 , GRCh37.p13 chr9: 16,421,495-16,426,142 BNC2
    nsv5866875copy number variation1nstd209human GRCh38 chr9: 16,464,513-16,468,843 , GRCh37.p13 chr9: 16,464,511-16,468,841 BNC2
    nsv5859391copy number variation1nstd209human GRCh38 chr9: 16,820,351-16,821,750 , GRCh37.p13 chr9: 16,820,349-16,821,748 BNC2
    nsv5858488copy number variation2nstd209human GRCh38 chr9: 16,422,436-16,424,235 , GRCh37.p13 chr9: 16,422,434-16,424,233 BNC2
    nsv5858381copy number variation1nstd209human GRCh38 chr9: 16,858,586-16,859,885 , GRCh37.p13 chr9: 16,858,584-16,859,883 BNC2
    nsv5857348copy number variation1nstd209human GRCh38 chr9: 16,502,897-16,504,596 , GRCh37.p13 chr9: 16,502,895-16,504,594 BNC2
    nsv5855443copy number variation1nstd209human GRCh38 chr9: 16,421,436-16,425,739 , GRCh37.p13 chr9: 16,421,434-16,425,737 BNC2
    nsv5852383copy number variation1nstd209human GRCh38 chr9: 16,461,546-16,463,853 , GRCh37.p13 chr9: 16,461,544-16,463,851 BNC2
    nsv5849281copy number variation1nstd209human GRCh38 chr9: 16,462,346-16,463,953 , GRCh37.p13 chr9: 16,462,344-16,463,951 BNC2
    nsv5726066mobile element insertion2nstd211human GRCh38 chr9: 16,749,176-16,749,176 , GRCh37.p13 chr9: 16,749,174-16,749,174 BNC2
    nsv5713368mobile element insertion2nstd211human GRCh38 chr9: 16,549,081-16,549,081 , GRCh37.p13 chr9: 16,549,079-16,549,079 BNC2
    nsv5705720mobile element insertion2nstd211human GRCh38 chr9: 16,443,556-16,443,556 , GRCh37.p13 chr9: 16,443,554-16,443,554 BNC2
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