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Items: 1 to 20 of 294

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957490insertion1nstd209human GRCh38 chr7: 45,641,932-45,641,932 , GRCh37.p13 chr7: 45,681,531-45,681,531 ADCY1
    nsv5950320insertion1nstd209human GRCh38 chr7: 45,696,151-45,696,151 , GRCh37.p13 chr7: 45,735,750-45,735,750 ADCY1
    nsv5907649copy number variation1nstd209human GRCh38 chr7: 45,352,020-45,696,175 , GRCh37.p13 chr7: 45,391,619-45,735,774 , ADCY1, 1 more genes
    nsv5685425mobile element insertion1nstd211human GRCh38 chr7: 45,637,763-45,637,763 , GRCh37.p13 chr7: 45,677,362-45,677,362 ADCY1
    nsv5682972mobile element insertion2nstd211human GRCh38 chr7: 45,643,304-45,643,304 , GRCh37.p13 chr7: 45,682,903-45,682,903 ADCY1
    nsv5635827insertion1nstd207human GRCh38 chr7: 45,711,880-45,711,880 , GRCh37.p13 chr7: 45,751,479-45,751,479 ADCY1
    nsv5632383insertion1nstd207human GRCh38 chr7: 45,611,031-45,611,031 , GRCh37.p13 chr7: 45,650,630-45,650,630 ADCY1
    nsv5629314insertion1nstd207human GRCh38 chr7: 45,610,760-45,610,760 , GRCh37.p13 chr7: 45,650,359-45,650,359 ADCY1
    nsv5628055insertion1nstd207human GRCh38 chr7: 45,611,281-45,611,281 , GRCh37.p13 chr7: 45,650,880-45,650,880 ADCY1
    nsv5556950sequence alteration1nstd206human GRCh38 chr7: 44,712,903-47,388,095 , GRCh37.p13 chr7: 44,752,502-47,427,692 , ADCY1, 51 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5551603insertion1nstd206human GRCh38 chr7: 45,696,150-45,696,156 , GRCh37.p13 chr7: 45,735,749-45,735,755 ADCY1
    nsv5488454copy number variation1nstd206human GRCh38 chr7: 45,589,372-45,589,889 , GRCh37.p13 chr7: 45,628,971-45,629,488 ADCY1
    nsv5484290copy number variation1nstd206human GRCh38 chr7: 45,655,783-45,656,008 , GRCh37.p13 chr7: 45,695,382-45,695,607 ADCY1
    nsv5411387mobile element insertion1nstd206human GRCh38 chr7: 45,637,763-45,637,814 , GRCh37.p13 chr7: 45,677,362-45,677,413 ADCY1
    nsv5408989mobile element insertion1nstd206human GRCh38 chr7: 45,643,304-45,643,355 , GRCh37.p13 chr7: 45,682,903-45,682,954 ADCY1
    nsv5381787copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,341,583-50,171,623 , GRCh38.p12 chr7: 43,301,984-50,132,027 OGDH, LOC112267918, 110 more genes
    nsv5381783copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969 ELK1P1, URGCP, 121 more genes
    nsv5370534translocation1nstd200human GRCh38 chr7: 45,610,699-45,610,699 , GRCh38 chr7: 45,611,113-45,611,113 , GRCh37.p13 chr7: 45,650,298-45,650,298 , GRCh37.p13 chr7: 45,650,712-45,650,712 ADCY1
    nsv5370533translocation1nstd200human GRCh38 chr7: 45,600,566-45,600,566 , GRCh38 chr7: 45,599,710-45,599,710 , GRCh37.p13 chr7: 45,639,309-45,639,309 , GRCh37.p13 chr7: 45,640,165-45,640,165 ADCY1
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