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Items: 1 to 20 of 546

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126947insertion1nstd186human GRCh37 chr7: 129,282,617-129,282,642 , GRCh38.p12 chr7: 129,642,776-129,642,801 NRF1
    nsv5965917insertion1nstd209human GRCh38 chr7: 129,642,756-129,642,756 , GRCh37.p13 chr7: 129,282,597-129,282,597 NRF1
    nsv5952116insertion1nstd209human GRCh38 chr7: 129,754,464-129,754,464 , GRCh37.p13 chr7: 129,394,304-129,394,304 NRF1, RNA5SP244
    nsv5914101copy number variation1nstd209human GRCh38 chr7: 129,660,224-129,662,162 , GRCh37.p13 chr7: 129,300,064-129,302,002 NRF1
    nsv5913743copy number variation1nstd209human GRCh38 chr7: 129,623,076-129,626,564 , GRCh37.p13 chr7: 129,262,917-129,266,405 NRF1
    nsv5864599copy number variation1nstd209human GRCh38 chr7: 129,660,245-129,662,187 , GRCh37.p13 chr7: 129,300,085-129,302,027 NRF1
    nsv5847984copy number variation1nstd209human GRCh38 chr7: 129,623,187-129,626,560 , GRCh37.p13 chr7: 129,263,028-129,266,401 NRF1
    nsv5643120insertion1nstd207human GRCh38 chr7: 129,642,756-129,642,756 , GRCh37.p13 chr7: 129,282,597-129,282,597 NRF1
    nsv5571249copy number variation1nstd207human GRCh38 chr7: 129,660,224-129,662,162 , GRCh37.p13 chr7: 129,300,064-129,302,002 NRF1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5537684insertion1nstd206human GRCh38 chr7: 129,642,776-129,642,801 , GRCh37.p13 chr7: 129,282,617-129,282,642 NRF1
    nsv5487017copy number variation1nstd206human GRCh38 chr7: 129,744,293-129,771,997 , GRCh37.p13 chr7: 129,384,133-129,411,837 NRF1, MIR182, 2 more genes
    nsv5485164copy number variation1nstd206human GRCh38 chr7: 129,659,715-129,662,145 , GRCh37.p13 chr7: 129,299,555-129,301,985 NRF1
    nsv5483857copy number variation1nstd206human GRCh38 chr7: 129,656,257-129,656,495 , GRCh37.p13 chr7: 129,296,097-129,296,335 NRF1
    nsv5483393copy number variation1nstd206human GRCh38 chr7: 129,628,032-129,628,099 , GRCh37.p13 chr7: 129,267,873-129,267,940 NRF1
    nsv5482015copy number variation1nstd206human GRCh38 chr7: 129,681,735-129,681,921 , GRCh37.p13 chr7: 129,321,575-129,321,761 NRF1
    nsv5474660copy number variation1nstd206human GRCh38 chr7: 129,645,902-129,646,750 , GRCh37.p13 chr7: 129,285,742-129,286,590 NRF1
    nsv5386458copy number variation2nstd186human GRCh37 chr7: 129,300,120-129,301,945 , GRCh38.p12 chr7: 129,660,280-129,662,105 NRF1
    nsv5378332translocation1nstd200human GRCh38 chr7: 129,631,122-129,631,122 , GRCh38 chr6: 29,720,862-29,720,862 , GRCh37.p13 chr6: 29,688,639-29,688,639 , GRCh37.p13 chr7: 129,270,963-129,270,963 NRF1, HCG4P11
    nsv5371205translocation1nstd200human GRCh38 chr7: 129,755,909-129,755,909 , GRCh38 chr7: 129,755,963-129,755,963 , GRCh37.p13 chr7: 129,395,749-129,395,749 , GRCh37.p13 chr7: 129,395,803-129,395,803 RNA5SP244, NRF1
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