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Items: 1 to 20 of 633

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137596insertion1nstd232human GRCh37.p13 chr2: 3,447,662-3,447,662 , GRCh38.p12 chr2: 3,443,891-3,443,891 , GRCh38.p12 chr2|NT_187522.1: 53,360-53,360 TRAPPC12
    nsv7096158copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,391,395-3,624,240 , GRCh38.p12 chr2: 3,387,624-3,576,650 , GRCh38.p12 chr2|NT_187522.1: 1-120,616 RPS7, RNASEH1-DT, 4 more genes
    nsv7096157copy number variation1nstd102humanPathogenic GRCh37 chr2: 3,391,395-3,428,454 , GRCh38.p12 chr2: 3,387,624-3,424,683 , GRCh38.p12 chr2|NT_187522.1: 1-34,747 TRAPPC12
    nsv7057382inversion1nstd229human GRCh38 chr2: 3,343,573-5,044,013 , GRCh37.p13 chr2: 3,347,344-5,184,146 RNASEH1-DT, LOC105373394, 19 more genes
    nsv7054663inversion1nstd229human GRCh38 chr2: 3,414,817-3,414,919 , GRCh37.p13 chr2: 3,418,588-3,418,690 TRAPPC12
    nsv7046124inversion1nstd229human GRCh38 chr2: 3,430,330-3,430,341 , GRCh37.p13 chr2: 3,434,101-3,434,112 TRAPPC12
    nsv7045549inversion1nstd229human GRCh38 chr2: 2,958,160-3,653,889 , GRCh37.p13 chr2: 2,961,932-3,701,479 EIPR1, RPS7, 10 more genes
    nsv7039393inversion1nstd229human GRCh38 chr2: 378,067-4,298,462 , GRCh37.p13 chr2: 378,067-4,346,052 LOC105373393, RPS7, 42 more genes
    nsv6676985copy number variation1nstd229human GRCh38 chr2: 3,156,357-3,467,904 , GRCh37.p13 chr2: 3,160,128-3,471,675 TRAPPC12, LOC107985840, 1 more genes
    nsv6676655copy number variation1nstd229human GRCh38 chr2: 3,424,005-3,428,880 , GRCh37.p13 chr2: 3,427,776-3,432,651 TRAPPC12
    nsv6675421copy number variation1nstd229human GRCh38 chr2: 3,335,801-3,388,723 , GRCh37.p13 chr2: 3,339,572-3,392,494 EIPR1, TRAPPC12
    nsv6675343copy number variation1nstd229human GRCh38 chr2: 3,406,600-3,412,098 , GRCh37.p13 chr2: 3,410,371-3,415,869 TRAPPC12
    nsv6673813copy number variation1nstd229human GRCh38 chr2: 3,382,766-3,385,381 , GRCh37.p13 chr2: 3,386,537-3,389,152 TRAPPC12
    nsv6673170copy number variation1nstd229human GRCh38 chr2: 3,418,301-3,651,400 , GRCh37.p13 chr2: 3,422,072-3,698,990 RNASEH1, ALLC, 7 more genes
    nsv6672438copy number variation1nstd229human GRCh38 chr2: 3,377,601-3,380,200 , GRCh37.p13 chr2: 3,381,372-3,383,971 TRAPPC12, EIPR1
    nsv6670847copy number variation1nstd229human GRCh38 chr2: 3,456,516-3,456,646 , GRCh37.p13 chr2: 3,460,287-3,460,417 TRAPPC12
    nsv6668874copy number variation1nstd229human GRCh38 chr2: 3,291,608-3,449,075 , GRCh37.p13 chr2: 3,295,379-3,452,846 TRAPPC12, EIPR1
    nsv6668670copy number variation1nstd229human GRCh38 chr2: 3,412,661-3,416,067 , GRCh37.p13 chr2: 3,416,432-3,419,838 TRAPPC12
    nsv6667193copy number variation1nstd229human GRCh38 chr2: 3,358,584-3,733,752 , GRCh37.p13 chr2: 3,362,355-3,781,342 GAPDHP48, RNASEH1-DT, 11 more genes
    nsv6667135copy number variation1nstd229human GRCh38 chr2: 3,466,743-3,477,782 , GRCh37.p13 chr2: 3,470,514-3,481,553 TRAPPC12
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