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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5715881mobile element insertion2nstd211human GRCh38 chr7: 107,914,402-107,914,402 , GRCh37.p13 chr7: 107,554,847-107,554,847 DLD
    nsv5642762insertion1nstd207human GRCh38 chr7: 107,901,921-107,901,921 , GRCh37.p13 chr7: 107,542,366-107,542,366 DLD
    nsv5563477mobile element insertion1nstd206human GRCh38 chr7: 107,914,402-107,914,453 , GRCh37.p13 chr7: 107,554,847-107,554,898 DLD
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5484136copy number variation1nstd206human GRCh38 chr7: 107,901,921-107,902,058 , GRCh37.p13 chr7: 107,542,366-107,542,503 DLD
    nsv5479657copy number variation1nstd206human GRCh38 chr7: 107,897,855-107,898,482 , GRCh37.p13 chr7: 107,538,300-107,538,927 DLD
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4705608copy number variation1nstd195human GRCh37 chr7: 107,489,501-107,769,251 , GRCh38.p12 chr7: 107,849,056-108,128,806 DLD, LAMB1, 6 more genes
    nsv4682811copy number variation1nstd102humanPathogenic GRCh37 chr7: 107,542,173-107,546,823 , GRCh38.p12 chr7: 107,901,728-107,906,378 DLD
    nsv4675821copy number variation1nstd102humanUncertain significance GRCh37 chr7: 107,441,501-108,433,812 , GRCh38.p12 chr7: 107,801,056-108,793,368 LOC105375444, LOC107986836, 18 more genes
    nsv4675322copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,617,406-123,217,914 , GRCh38.p12 chr7: 106,976,961-123,577,860 CBLL1-AS1, COMETT, 168 more genes
    nsv4558799mobile element insertion1nstd166human GRCh37.p13 chr7: 107,554,832-107,554,832 , GRCh38.p12 chr7: 107,914,387-107,914,387 DLD
    nsv4494999mobile element insertion1nstd166human GRCh37.p13 chr7: 107,533,774-107,533,774 , GRCh38.p12 chr7: 107,893,329-107,893,329 DLD
    nsv4455557copy number variation1nstd102humanPathogenic GRCh37 chr7: 107,410,314-117,825,549 , GRCh38.p12 chr7: 107,769,869-118,185,495 RAC1P6, LOC101928012, 103 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4160424copy number variation1nstd166human GRCh37.p13 chr7: 107,542,366-107,542,503 , GRCh38.p12 chr7: 107,901,921-107,902,058 DLD
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