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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960904insertion1nstd209human GRCh38 chr6: 167,130,973-167,130,973 , GRCh37.p13 chr6: 167,544,461-167,544,461 CCR6
    nsv5908391copy number variation1nstd209human GRCh38 chr6: 167,129,525-167,130,939 , GRCh37.p13 chr6: 167,543,013-167,544,427 CCR6
    nsv5844197copy number variation1nstd209human GRCh38 chr6: 167,129,523-167,130,952 , GRCh37.p13 chr6: 167,543,011-167,544,440 CCR6
    nsv5642390insertion1nstd207human GRCh38 chr6: 167,130,932-167,130,932 , GRCh37.p13 chr6: 167,544,420-167,544,420 CCR6
    nsv5642172insertion1nstd207human GRCh38 chr6: 167,130,970-167,130,970 , GRCh37.p13 chr6: 167,544,458-167,544,458 CCR6
    nsv5565600copy number variation1nstd207human GRCh38 chr6: 167,129,525-167,130,939 , GRCh37.p13 chr6: 167,543,013-167,544,427 CCR6
    nsv5541660insertion1nstd206human GRCh38 chr6: 167,130,947-167,130,976 , GRCh37.p13 chr6: 167,544,435-167,544,464 CCR6
    nsv5538615insertion1nstd206human GRCh38 chr6: 167,131,012-167,131,023 , GRCh37.p13 chr6: 167,544,500-167,544,511 CCR6
    nsv5471514copy number variation1nstd206human GRCh38 chr6: 167,114,066-167,117,048 , GRCh37.p13 chr6: 167,527,554-167,530,536 , CCR6
    nsv5457825copy number variation1nstd206human GRCh38 chr6: 167,129,527-167,130,940 , GRCh37.p13 chr6: 167,543,015-167,544,428 CCR6
    nsv5457188copy number variation1nstd206human GRCh38 chr6: 167,117,409-167,117,713 , GRCh37.p13 chr6: 167,530,897-167,531,201 , CCR6
    nsv5363549translocation1nstd200human GRCh38 chr6: 167,327,374-167,327,374 , GRCh38 chr6: 167,126,968-167,126,968 , GRCh37.p13 chr6: 167,740,862-167,740,862 , GRCh37.p13 chr6: 167,540,456-167,540,456 CCR6, TTLL2, 1 more genes
    nsv5339200translocation1nstd200human GRCh37 chr6: 167,540,456-167,540,456 , GRCh37 chr6: 167,740,862-167,740,862 , GRCh38.p12 chr6: 167,126,968-167,126,968 , GRCh38.p12 chr6: 167,327,374-167,327,374 CCR6, TTLL2, 1 more genes
    nsv5304613copy number variation1nstd204human GRCh38.p13 chr6: 167,129,505-167,130,960 , GRCh37.p13 chr6: 167,542,993-167,544,448 CCR6
    nsv5240083copy number variation1nstd204human GRCh38.p13 chr6: 167,129,501-167,130,700 , GRCh37.p13 chr6: 167,542,989-167,544,188 CCR6
    nsv5239323copy number variation1nstd204human GRCh38.p13 chr6: 167,129,623-167,130,722 , GRCh37.p13 chr6: 167,543,111-167,544,210 CCR6
    nsv4965954copy number variation1nstd200human GRCh38 chr6: 167,129,527-167,130,940 , GRCh37.p13 chr6: 167,543,015-167,544,428 CCR6
    nsv4965953copy number variation1nstd200human GRCh38 chr6: 167,113,616-167,115,246 , GRCh37.p13 chr6: 167,527,104-167,528,734 , CCR6
    nsv4965952copy number variation1nstd200human GRCh38 chr6: 167,107,458-167,110,695 , GRCh37.p13 chr6: 167,520,946-167,524,183 , CCR6
    nsv4870713mobile element deletion1nstd200human GRCh38 chr6: 167,117,409-167,117,713 , GRCh37.p13 chr6: 167,530,897-167,531,201 , CCR6
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