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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975022inversion1nstd209human GRCh38 chr7: 34,818,028-37,653,165 , GRCh37.p13 chr7: 34,857,640-37,692,768 , AOAH, 41 more genes
    nsv5920411copy number variation1nstd209human GRCh38 chr7: 35,631,438-35,631,657 , GRCh37.p13 chr7: 35,671,048-35,671,267 HERPUD2, LOC101928421
    nsv5914132copy number variation1nstd209human GRCh38 chr7: 26,936,027-36,716,695 , GRCh37.p13 chr7: 26,975,646-36,756,300 , HOXA7, 162 more genes
    nsv5912678copy number variation1nstd209human GRCh38 chr7: 35,631,748-35,631,809 , GRCh37.p13 chr7: 35,671,358-35,671,419 HERPUD2, LOC101928421
    nsv5683353mobile element insertion1nstd211human GRCh38 chr7: 35,653,322-35,653,322 , GRCh37.p13 chr7: 35,692,932-35,692,932 HERPUD2
    nsv5639709insertion1nstd207human GRCh38 chr7: 35,682,326-35,682,326 , GRCh37.p13 chr7: 35,721,936-35,721,936 HERPUD2
    nsv5582251copy number variation1nstd207human GRCh38 chr7: 35,631,826-35,631,879 , GRCh37.p13 chr7: 35,671,436-35,671,489 HERPUD2, LOC101928421
    nsv5573524copy number variation1nstd207human GRCh38 chr7: 35,682,268-35,682,325 , GRCh37.p13 chr7: 35,721,878-35,721,935 HERPUD2
    nsv5570510copy number variation1nstd207human GRCh38 chr7: 35,632,266-35,632,316 , GRCh37.p13 chr7: 35,671,876-35,671,926 HERPUD2
    nsv5565259copy number variation1nstd207human GRCh38 chr7: 35,631,435-35,631,654 , GRCh37.p13 chr7: 35,671,045-35,671,264 HERPUD2, LOC101928421
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5488706copy number variation1nstd206human GRCh38 chr7: 35,631,438-35,631,660 , GRCh37.p13 chr7: 35,671,048-35,671,270 LOC101928421, HERPUD2
    nsv5484326copy number variation1nstd206human GRCh38 chr7: 35,682,101-35,685,358 , GRCh37.p13 chr7: 35,721,711-35,724,968 HERPUD2
    nsv5483476copy number variation1nstd206human GRCh38 chr7: 35,633,028-35,633,117 , GRCh37.p13 chr7: 35,672,638-35,672,727 HERPUD2
    nsv5394782mobile element insertion1nstd206human GRCh38 chr7: 35,653,322-35,653,373 , GRCh37.p13 chr7: 35,692,932-35,692,983 HERPUD2
    nsv5389092copy number variation3nstd186human GRCh37 chr7: 35,671,048-35,671,270 , GRCh38.p12 chr7: 35,631,438-35,631,660 HERPUD2, LOC101928421
    nsv5378658translocation1nstd200human GRCh38 chr7: 35,685,358-35,685,358 , GRCh38 chr7: 35,682,101-35,682,101 , GRCh37.p13 chr7: 35,724,968-35,724,968 , GRCh37.p13 chr7: 35,721,711-35,721,711 HERPUD2
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4966171copy number variation1nstd200human GRCh38 chr7: 35,631,438-35,631,660 , GRCh37.p13 chr7: 35,671,048-35,671,270 HERPUD2, LOC101928421
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
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