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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977401insertion1nstd209human GRCh38 chr16: 69,713,893-69,713,893 , GRCh37.p13 chr16: 69,747,796-69,747,796 NQO1
    nsv5532278copy number variation1nstd206human GRCh38 chr16: 69,677,060-69,924,863 , GRCh37.p13 chr16: 69,710,963-69,958,766 NQO1, NFAT5, 4 more genes
    nsv5519294copy number variation1nstd206human GRCh38 chr16: 69,710,106-69,714,771 , GRCh37.p13 chr16: 69,744,009-69,748,674 NQO1
    nsv5263716copy number variation1nstd204human GRCh37.p13 chr16: 69,700,104-69,946,603 , GRCh38.p13 chr16: 69,666,201-69,912,700 NQO1, NFAT5, 4 more genes
    nsv5157524mobile element insertion1nstd203human GRCh38 chr16: 69,713,888-69,713,941 , GRCh37.p13 chr16: 69,747,791-69,747,844 NQO1
    nsv5157381mobile element insertion1nstd203human GRCh38 chr16: 69,713,871-69,713,888 , GRCh37.p13 chr16: 69,747,774-69,747,791 NQO1
    nsv5154237mobile element insertion1nstd203human GRCh38 chr16: 69,713,882-69,713,893 , GRCh37.p13 chr16: 69,747,785-69,747,796 NQO1
    nsv5153654mobile element insertion1nstd203human GRCh38 chr16: 69,713,764-69,713,764 , GRCh37.p13 chr16: 69,747,667-69,747,667 NQO1
    nsv5151522mobile element insertion1nstd203human GRCh38 chr16: 69,713,891-69,713,903 , GRCh37.p13 chr16: 69,747,794-69,747,806 NQO1
    nsv5150678mobile element insertion1nstd203human GRCh38 chr16: 69,713,897-69,713,939 , GRCh37.p13 chr16: 69,747,800-69,747,842 NQO1
    nsv5149490mobile element insertion1nstd203human GRCh38 chr16: 69,713,890-69,713,903 , GRCh37.p13 chr16: 69,747,793-69,747,806 NQO1
    nsv5144987mobile element insertion1nstd203human GRCh38 chr16: 69,713,893-69,713,903 , GRCh37.p13 chr16: 69,747,796-69,747,806 NQO1
    nsv5144561mobile element insertion1nstd203human GRCh38 chr16: 69,714,145-69,714,181 , GRCh37.p13 chr16: 69,748,048-69,748,084 NQO1
    nsv5140941mobile element insertion1nstd203human GRCh38 chr16: 69,713,873-69,713,893 , GRCh37.p13 chr16: 69,747,776-69,747,796 NQO1
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5005810copy number variation1nstd200human GRCh38 chr16: 69,714,838-69,715,847 , GRCh37.p13 chr16: 69,748,741-69,749,750 NQO1
    nsv4993216copy number variation1nstd200human GRCh38 chr16: 69,710,106-69,714,781 , GRCh37.p13 chr16: 69,744,009-69,748,684 NQO1
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4857554copy number variation1nstd200human GRCh37 chr16: 69,750,370-69,752,840 , GRCh38.p12 chr16: 69,716,467-69,718,937 NQO1
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
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