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Items: 1 to 20 of 297

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963528insertion1nstd209human GRCh38 chr7: 104,195,017-104,195,017 , GRCh37.p13 chr7: 103,835,465-103,835,465 ORC5
    nsv5961448insertion1nstd209human GRCh38 chr7: 104,191,580-104,191,580 , GRCh37.p13 chr7: 103,832,028-103,832,028 ORC5
    nsv5927348copy number variation1nstd209human GRCh38 chr7: 104,158,966-104,159,021 , GRCh37.p13 chr7: 103,799,414-103,799,469 ORC5
    nsv5908747copy number variation1nstd209human GRCh38 chr7: 104,131,789-104,134,351 , GRCh37.p13 chr7: 103,772,236-103,774,798 ORC5
    nsv5855798copy number variation3nstd209human GRCh38 chr7: 104,204,296-104,206,681 , GRCh37.p13 chr7: 103,844,744-103,847,129 ORC5
    nsv5849840copy number variation1nstd209human GRCh38 chr7: 104,131,923-104,134,422 , GRCh37.p13 chr7: 103,772,370-103,774,869 ORC5
    nsv5691531mobile element insertion1nstd211human GRCh38 chr7: 104,181,418-104,181,418 , GRCh37.p13 chr7: 103,821,866-103,821,866 ORC5
    nsv5680725mobile element insertion2nstd211human GRCh38 chr7: 104,191,595-104,191,595 , GRCh37.p13 chr7: 103,832,043-103,832,043 ORC5
    nsv5678779mobile element insertion2nstd211human GRCh38 chr7: 104,168,669-104,168,669 , GRCh37.p13 chr7: 103,809,117-103,809,117 ORC5
    nsv5583549copy number variation1nstd207human GRCh38 chr7: 104,158,966-104,159,021 , GRCh37.p13 chr7: 103,799,414-103,799,469 ORC5
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5550943insertion1nstd206human GRCh38 chr7: 104,195,038-104,195,068 , GRCh37.p13 chr7: 103,835,486-103,835,516 ORC5
    nsv5538246insertion1nstd206human GRCh38 chr7: 104,191,595-104,191,597 , GRCh37.p13 chr7: 103,832,043-103,832,045 ORC5
    nsv5493069copy number variation1nstd206human GRCh38 chr7: 104,097,187-104,361,255 , GRCh37.p13 chr7: 103,737,634-104,001,703 ORC5, LHFPL3
    nsv5489881copy number variation1nstd206human GRCh38 chr7: 104,131,837-104,134,349 , GRCh37.p13 chr7: 103,772,284-103,774,796 ORC5
    nsv5484017copy number variation1nstd206human GRCh38 chr7: 104,178,400-104,178,476 , GRCh37.p13 chr7: 103,818,848-103,818,924 ORC5
    nsv5412484mobile element insertion1nstd206human GRCh38 chr7: 104,190,737-104,190,788 , GRCh37.p13 chr7: 103,831,185-103,831,236 ORC5
    nsv5408337mobile element insertion1nstd206human GRCh38 chr7: 104,168,669-104,168,720 , GRCh37.p13 chr7: 103,809,117-103,809,168 ORC5
    nsv5399929mobile element insertion1nstd206human GRCh38 chr7: 104,181,418-104,181,469 , GRCh37.p13 chr7: 103,821,866-103,821,917 ORC5
    nsv5336033translocation1nstd200human GRCh37 chr7: 103,798,430-103,798,430 , GRCh37 chr7: 103,798,504-103,798,504 , GRCh38.p12 chr7: 104,157,982-104,157,982 , GRCh38.p12 chr7: 104,158,056-104,158,056 ORC5
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