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Items: 1 to 20 of 608

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966789insertion1nstd209human GRCh38 chr2: 172,798,635-172,798,635 , GRCh37.p13 chr2: 173,663,363-173,663,363 RAPGEF4
    nsv5965340insertion1nstd209human GRCh38 chr2: 172,831,266-172,831,266 , GRCh37.p13 chr2: 173,695,994-173,695,994 RAPGEF4
    nsv5902665copy number variation1nstd209human GRCh38 chr2: 172,953,576-172,953,699 , GRCh37.p13 chr2: 173,818,304-173,818,427 RAPGEF4
    nsv5896751copy number variation1nstd209human GRCh38 chr2: 172,838,084-172,839,708 , GRCh37.p13 chr2: 173,702,812-173,704,436 RAPGEF4
    nsv5832014copy number variation1nstd209human GRCh38 chr2: 172,838,156-172,839,755 , GRCh37.p13 chr2: 173,702,884-173,704,483 RAPGEF4
    nsv5727826mobile element insertion2nstd211human GRCh38 chr2: 172,989,382-172,989,382 , GRCh37.p13 chr2: 173,854,110-173,854,110 RAPGEF4
    nsv5679638mobile element insertion1nstd211human GRCh38 chr2: 172,790,380-172,790,380 , GRCh37.p13 chr2: 173,655,108-173,655,108 RAPGEF4
    nsv5676082mobile element insertion2nstd211human GRCh38 chr2: 172,752,438-172,752,438 , GRCh37.p13 chr2: 173,617,166-173,617,166 RAPGEF4
    nsv5623965insertion1nstd207human GRCh38 chr2: 172,798,635-172,798,635 , GRCh37.p13 chr2: 173,663,363-173,663,363 RAPGEF4
    nsv5580181copy number variation1nstd207human GRCh38 chr2: 173,024,192-173,024,515 , GRCh37.p13 chr2: 173,888,920-173,889,243 RAPGEF4
    nsv5561266mobile element insertion1nstd206human GRCh38 chr2: 172,989,382-172,989,433 , GRCh37.p13 chr2: 173,854,110-173,854,161 RAPGEF4
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5536573insertion1nstd206human GRCh38 chr2: 172,798,648-172,798,686 , GRCh37.p13 chr2: 173,663,376-173,663,414 RAPGEF4
    nsv5448166copy number variation1nstd206human GRCh38 chr2: 172,838,087-172,839,709 , GRCh37.p13 chr2: 173,702,815-173,704,437 RAPGEF4
    nsv5438590copy number variation1nstd206human GRCh38 chr2: 173,024,207-173,024,516 , GRCh37.p13 chr2: 173,888,935-173,889,244 RAPGEF4
    nsv5438322copy number variation1nstd206human GRCh38 chr2: 172,945,347-172,945,457 , GRCh37.p13 chr2: 173,810,075-173,810,185 RAPGEF4
    nsv5437614copy number variation1nstd206human GRCh38 chr2: 172,743,646-172,750,549 , GRCh37.p13 chr2: 173,608,374-173,615,277 RAPGEF4
    nsv5394582mobile element insertion1nstd206human GRCh38 chr2: 172,752,438-172,752,458 , GRCh37.p13 chr2: 173,617,166-173,617,186 RAPGEF4
    nsv5383076mobile element deletion2nstd186human GRCh37 chr2: 173,888,935-173,889,244 , GRCh38.p12 chr2: 173,024,207-173,024,516 RAPGEF4
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