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Items: 1 to 20 of 159

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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
    nsv5958148insertion1nstd209human GRCh38 chr7: 35,252,129-35,252,129 , GRCh37.p13 chr7: 35,291,740-35,291,740 TBX20
    nsv5914132copy number variation1nstd209human GRCh38 chr7: 26,936,027-36,716,695 , GRCh37.p13 chr7: 26,975,646-36,756,300 , HOXA7, 162 more genes
    nsv5640988insertion1nstd207human GRCh38 chr7: 35,203,776-35,203,776 , GRCh37.p13 chr7: 35,243,388-35,243,388 TBX20
    nsv5583189copy number variation1nstd207human GRCh38 chr7: 35,224,516-35,224,591 , GRCh37.p13 chr7: 35,264,128-35,264,203 TBX20
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5378655translocation1nstd200human GRCh38 chr7: 35,247,768-35,247,768 , GRCh38 chr7: 35,246,322-35,246,322 , GRCh37.p13 chr7: 35,287,380-35,287,380 , GRCh37.p13 chr7: 35,285,934-35,285,934 TBX20
    nsv5378654translocation1nstd200human GRCh38 chr7: 35,222,732-35,222,732 , GRCh38 chr7: 35,223,667-35,223,667 , GRCh37.p13 chr7: 35,262,344-35,262,344 , GRCh37.p13 chr7: 35,263,279-35,263,279 TBX20
    nsv5341780translocation1nstd200human GRCh37 chr7: 35,262,344-35,262,344 , GRCh37 chr7: 35,263,279-35,263,279 , GRCh38.p12 chr7: 35,223,667-35,223,667 , GRCh38.p12 chr7: 35,222,732-35,222,732 TBX20
    nsv5114500mobile element insertion1nstd203human GRCh38 chr7: 35,214,836-35,214,851 , GRCh37.p13 chr7: 35,254,448-35,254,463 TBX20
    nsv5106604mobile element insertion1nstd203human GRCh38 chr7: 35,228,397-35,228,397 , GRCh37.p13 chr7: 35,268,009-35,268,009 TBX20
    nsv5100969mobile element insertion1nstd203human GRCh38 chr7: 35,208,742-35,208,782 , GRCh37.p13 chr7: 35,248,354-35,248,394 TBX20
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956344copy number variation1nstd200human GRCh38 chr7: 35,207,390-35,208,602 , GRCh37.p13 chr7: 35,247,002-35,248,214 TBX20
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4811308copy number variation1nstd200human GRCh37 chr7: 35,285,934-35,287,380 , GRCh38.p12 chr7: 35,246,322-35,247,768 TBX20
    nsv4811307copy number variation1nstd200human GRCh37 chr7: 35,247,002-35,248,214 , GRCh38.p12 chr7: 35,207,390-35,208,602 TBX20
    nsv4769379copy number variation1nstd102humanUncertain significance GRCh37 chr7: 34,937,625-35,241,685 , GRCh38.p12 chr7: 34,898,013-35,202,073 DPY19L1, MIR548N, 5 more genes
    nsv4714742translocation1nstd195human GRCh37 chr7: 35,237,943-35,237,943 , GRCh37 chr12: 64,074,509-64,074,509 , GRCh38.p12 chr12: 63,680,729-63,680,729 , GRCh38.p12 chr7: 35,198,331-35,198,331 TBX20
    nsv4675010copy number variation1nstd102humanUncertain significance GRCh37 chr7: 34,859,227-35,374,178 , GRCh38.p12 chr7: 34,819,615-35,334,568 LOC102724723, MIR548N, 8 more genes
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