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Items: 1 to 20 of 316

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977436insertion1nstd209human GRCh38 chr12: 51,149,024-51,149,024 , GRCh37.p13 chr12: 51,542,807-51,542,807 TFCP2
    nsv5944623copy number variation1nstd209human GRCh38 chr12: 51,147,283-51,148,639 , GRCh37.p13 chr12: 51,541,066-51,542,422 TFCP2
    nsv5655281insertion1nstd207human GRCh38 chr12: 51,147,274-51,147,274 , GRCh37.p13 chr12: 51,541,057-51,541,057 TFCP2
    nsv5589192copy number variation1nstd207human GRCh38 chr12: 51,132,298-51,132,370 , GRCh37.p13 chr12: 51,526,081-51,526,153 TFCP2
    nsv5556240sequence alteration1nstd206human GRCh38 chr12: 50,501,429-51,116,796 , GRCh37.p13 chr12: 50,895,212-51,510,579 ATF1, SLC11A2, 14 more genes
    nsv5506728copy number variation1nstd206human GRCh38 chr12: 51,144,128-51,150,128 , GRCh37.p13 chr12: 51,537,911-51,543,911 TFCP2
    nsv5502351copy number variation1nstd206human GRCh38 chr12: 51,119,508-51,119,936 , GRCh37.p13 chr12: 51,513,291-51,513,719 TFCP2
    nsv5496534copy number variation1nstd206human GRCh38 chr12: 51,141,769-51,141,952 , GRCh37.p13 chr12: 51,535,552-51,535,735 TFCP2
    nsv5496326copy number variation1nstd206human GRCh38 chr12: 51,147,268-51,148,674 , GRCh37.p13 chr12: 51,541,051-51,542,457 TFCP2
    nsv5494790copy number variation1nstd206human GRCh38 chr12: 51,145,367-51,150,142 , GRCh37.p13 chr12: 51,539,150-51,543,925 TFCP2
    nsv5310056copy number variation1nstd204human GRCh38.p13 chr12: 51,146,911-51,149,075 , GRCh37.p13 chr12: 51,540,694-51,542,858 TFCP2
    nsv5302479copy number variation1nstd204human GRCh38.p13 chr12: 51,132,295-51,132,376 , GRCh37.p13 chr12: 51,526,078-51,526,159 TFCP2
    nsv5264015copy number variation1nstd204human GRCh38.p13 chr12: 51,084,501-51,093,500 , GRCh37.p13 chr12: 51,478,284-51,487,283 TFCP2
    nsv5192942mobile element insertion1nstd203human GRCh38 chr12: 51,098,112-51,098,128 , GRCh37.p13 chr12: 51,491,895-51,491,911 TFCP2
    nsv5189859mobile element insertion1nstd203human GRCh38 chr12: 51,149,553-51,149,566 , GRCh37.p13 chr12: 51,543,336-51,543,349 TFCP2
    nsv5133673mobile element insertion1nstd203human GRCh38 chr12: 51,092,680-51,092,695 , GRCh37.p13 chr12: 51,486,463-51,486,478 TFCP2
    nsv5126392mobile element insertion1nstd203human GRCh38 chr12: 51,104,318-51,104,335 , GRCh37.p13 chr12: 51,498,101-51,498,118 TFCP2
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4985589copy number variation1nstd200human GRCh38 chr12: 51,148,745-51,150,179 , GRCh37.p13 chr12: 51,542,528-51,543,962 TFCP2
    nsv4972662copy number variation1nstd200human GRCh38 chr12: 51,147,306-51,148,599 , GRCh37.p13 chr12: 51,541,089-51,542,382 TFCP2
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