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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124049insertion1nstd186human GRCh37 chr2: 56,101,135-56,101,181 , GRCh38.p12 chr2: 55,874,000-55,874,046 EFEMP1, LOC112268416
    nsv5968604inversion1nstd209human GRCh38 chr2: 49,436,021-59,087,697 , GRCh37.p13 chr2: 49,663,159-59,314,832 , ACYP2, 95 more genes
    nsv5956975insertion1nstd209human GRCh38 chr2: 55,873,983-55,873,983 , GRCh37.p13 chr2: 56,101,118-56,101,118 EFEMP1, LOC112268416
    nsv5879660copy number variation1nstd209human GRCh38 chr2: 55,919,393-55,919,459 , GRCh37.p13 chr2: 56,146,528-56,146,594 EFEMP1
    nsv5677364mobile element insertion2nstd211human GRCh38 chr2: 55,874,000-55,874,000 , GRCh37.p13 chr2: 56,101,135-56,101,135 LOC112268416, EFEMP1
    nsv5614301insertion1nstd207human GRCh38 chr2: 55,873,983-55,873,983 , GRCh37.p13 chr2: 56,101,118-56,101,118 EFEMP1, LOC112268416
    nsv5606258insertion1nstd207human GRCh38 chr2: 55,865,188-55,865,188 , GRCh37.p13 chr2: 56,092,323-56,092,323 EFEMP1, LOC112268416
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5541931insertion1nstd206human GRCh38 chr2: 55,874,000-55,874,046 , GRCh37.p13 chr2: 56,101,135-56,101,181 LOC112268416, EFEMP1
    nsv5077600mobile element insertion1nstd203human GRCh38 chr2: 55,873,988-55,874,000 , GRCh37.p13 chr2: 56,101,123-56,101,135 EFEMP1, LOC112268416
    nsv5077187mobile element insertion1nstd203human GRCh38 chr2: 55,873,986-55,874,000 , GRCh37.p13 chr2: 56,101,121-56,101,135 EFEMP1, LOC112268416
    nsv5077045mobile element insertion1nstd203human GRCh38 chr2: 55,874,000-55,874,000 , GRCh37.p13 chr2: 56,101,135-56,101,135 EFEMP1, LOC112268416
    nsv5066185mobile element insertion1nstd203human GRCh38 chr2: 55,873,994-55,874,000 , GRCh37.p13 chr2: 56,101,129-56,101,135 EFEMP1, LOC112268416
    nsv5065145mobile element insertion1nstd203human GRCh38 chr2: 55,873,990-55,874,000 , GRCh37.p13 chr2: 56,101,125-56,101,135 EFEMP1, LOC112268416
    nsv5062849mobile element insertion1nstd203human GRCh38 chr2: 55,873,983-55,874,000 , GRCh37.p13 chr2: 56,101,118-56,101,135 LOC112268416, EFEMP1
    nsv5061999mobile element insertion1nstd203human GRCh38 chr2: 55,873,985-55,874,000 , GRCh37.p13 chr2: 56,101,120-56,101,135 LOC112268416, EFEMP1
    nsv5030738inversion1nstd200human GRCh38 chr2: 53,702,002-58,642,705 , GRCh37.p13 chr2: 53,929,139-58,869,840 , LINC01122, 71 more genes
    nsv5030307inversion1nstd200human GRCh38 chr2: 48,550,793-61,622,055 , GRCh37.p13 chr2: 48,777,932-61,849,190 , MIR217, 146 more genes
    nsv4892808copy number variation1nstd200human GRCh38 chr2: 55,895,728-55,897,434 , GRCh37.p13 chr2: 56,122,863-56,124,569 EFEMP1
    nsv4770232copy number variation1nstd200human GRCh37 chr2: 56,122,854-56,124,563 , GRCh38.p12 chr2: 55,895,719-55,897,428 EFEMP1
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