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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5907220copy number variation1nstd209human GRCh38 chr4: 79,972,946-79,976,420 , GRCh37.p13 chr4: 80,894,100-80,897,574 ANTXR2
    nsv5897877copy number variation1nstd209human GRCh38 chr4: 80,015,893-80,015,942 , GRCh37.p13 chr4: 80,937,047-80,937,096 ANTXR2
    nsv5896400copy number variation1nstd209human GRCh38 chr4: 79,936,371-79,936,444 , GRCh37.p13 chr4: 80,857,525-80,857,598 ANTXR2
    nsv5892928copy number variation1nstd209human GRCh38 chr4: 79,966,892-79,972,936 , GRCh37.p13 chr4: 80,888,046-80,894,090 ANTXR2
    nsv5840125copy number variation1nstd209human GRCh38 chr4: 79,973,474-79,976,123 , GRCh37.p13 chr4: 80,894,628-80,897,277 ANTXR2
    nsv5726207mobile element insertion1nstd211human GRCh38 chr4: 79,933,752-79,933,752 , GRCh37.p13 chr4: 80,854,906-80,854,906 ANTXR2
    nsv5721735mobile element insertion1nstd211human GRCh38 chr4: 80,028,477-80,028,477 , GRCh37.p13 chr4: 80,949,631-80,949,631 ANTXR2
    nsv5720840mobile element insertion1nstd211human GRCh38 chr4: 79,966,876-79,966,876 , GRCh37.p13 chr4: 80,888,030-80,888,030 ANTXR2
    nsv5692195mobile element insertion1nstd211human GRCh38 chr4: 79,973,321-79,973,321 , GRCh37.p13 chr4: 80,894,475-80,894,475 ANTXR2
    nsv5691221mobile element insertion2nstd211human GRCh38 chr4: 79,917,944-79,917,944 , GRCh37.p13 chr4: 80,839,098-80,839,098 ANTXR2
    nsv5681703mobile element insertion2nstd211human GRCh38 chr4: 79,962,339-79,962,339 , GRCh37.p13 chr4: 80,883,493-80,883,493 ANTXR2
    nsv5622514insertion1nstd207human GRCh38 chr4: 79,917,937-79,917,937 , GRCh37.p13 chr4: 80,839,091-80,839,091 ANTXR2
    nsv5615877insertion1nstd207human GRCh38 chr4: 79,926,976-79,926,976 , GRCh37.p13 chr4: 80,848,130-80,848,130 ANTXR2
    nsv5607240insertion1nstd207human GRCh38 chr4: 79,936,371-79,936,371 , GRCh37.p13 chr4: 80,857,525-80,857,525 ANTXR2
    nsv5574849copy number variation1nstd207human GRCh38 chr4: 80,015,893-80,015,942 , GRCh37.p13 chr4: 80,937,047-80,937,096 ANTXR2
    nsv5569921copy number variation1nstd207human GRCh38 chr4: 79,966,892-79,972,936 , GRCh37.p13 chr4: 80,888,046-80,894,090 ANTXR2
    nsv5563284mobile element insertion1nstd206human GRCh38 chr4: 80,028,477-80,028,528 , GRCh37.p13 chr4: 80,949,631-80,949,682 ANTXR2
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5552457insertion1nstd206human GRCh38 chr4: 79,917,937-79,917,937 , GRCh37.p13 chr4: 80,839,091-80,839,091 ANTXR2
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
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