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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5892676copy number variation1nstd209human GRCh38 chr6: 46,622,560-46,622,621 , GRCh37.p13 chr6: 46,590,297-46,590,358 CYP39A1
    nsv5891493copy number variation1nstd209human GRCh38 chr6: 46,638,140-46,638,254 , GRCh37.p13 chr6: 46,605,877-46,605,991 CYP39A1
    nsv5890906copy number variation1nstd209human GRCh38 chr6: 46,629,865-46,631,295 , GRCh37.p13 chr6: 46,597,602-46,599,032 CYP39A1
    nsv5845621copy number variation1nstd209human GRCh38 chr6: 46,629,792-46,631,327 , GRCh37.p13 chr6: 46,597,529-46,599,064 CYP39A1
    nsv5674388mobile element insertion2nstd211human GRCh38 chr6: 46,632,977-46,632,977 , GRCh37.p13 chr6: 46,600,714-46,600,714 CYP39A1
    nsv5570671copy number variation1nstd207human GRCh38 chr6: 46,616,165-46,616,214 , GRCh37.p13 chr6: 46,583,902-46,583,951 CYP39A1
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5471869copy number variation1nstd206human GRCh38 chr6: 46,629,867-46,631,296 , GRCh37.p13 chr6: 46,597,604-46,599,033 CYP39A1
    nsv5459449copy number variation1nstd206human GRCh38 chr6: 46,622,560-46,622,622 , GRCh37.p13 chr6: 46,590,297-46,590,359 CYP39A1
    nsv5398535mobile element insertion1nstd206human GRCh38 chr6: 46,632,977-46,632,981 , GRCh37.p13 chr6: 46,600,714-46,600,718 CYP39A1
    nsv5362922translocation1nstd200human GRCh38 chr6: 46,629,867-46,629,867 , GRCh38 chr6: 46,631,296-46,631,296 , GRCh37.p13 chr6: 46,599,033-46,599,033 , GRCh37.p13 chr6: 46,597,604-46,597,604 CYP39A1
    nsv5342342translocation1nstd200human GRCh37 chr6: 46,597,604-46,597,604 , GRCh37 chr6: 46,599,033-46,599,033 , GRCh38.p12 chr6: 46,629,867-46,629,867 , GRCh38.p12 chr6: 46,631,296-46,631,296 CYP39A1
    nsv5237454copy number variation1nstd204human GRCh38.p13 chr6: 46,593,501-46,596,500 , GRCh37.p13 chr6: 46,561,238-46,564,237 CYP39A1
    nsv5170615mobile element insertion1nstd203human GRCh38 chr6: 46,570,240-46,570,258 , GRCh37.p13 chr6: 46,537,977-46,537,995 CYP39A1
    nsv5114887mobile element insertion1nstd203human GRCh38 chr6: 46,632,969-46,632,977 , GRCh37.p13 chr6: 46,600,706-46,600,714 CYP39A1
    nsv5109035mobile element insertion1nstd203human GRCh38 chr6: 46,645,082-46,645,094 , GRCh37.p13 chr6: 46,612,819-46,612,831 CYP39A1
    nsv4941241copy number variation1nstd200human GRCh38 chr6: 46,595,113-46,595,268 , GRCh37.p13 chr6: 46,562,850-46,563,005 CYP39A1
    nsv4816284copy number variation1nstd200human GRCh37 chr6: 46,605,881-46,605,992 , GRCh38.p12 chr6: 46,638,144-46,638,255 CYP39A1
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
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