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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127390insertion1nstd186human GRCh37 chr4: 154,084,965-154,085,001 , GRCh38.p12 chr4: 153,163,813-153,163,849 TRIM2
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5967898inversion1nstd209human GRCh38 chr4: 153,196,255-153,198,163 , GRCh37.p13 chr4: 154,117,407-154,119,315 TRIM2
    nsv5967068insertion1nstd209human GRCh38 chr4: 153,163,798-153,163,798 , GRCh37.p13 chr4: 154,084,950-154,084,950 TRIM2
    nsv5965242insertion1nstd209human GRCh38 chr4: 153,222,046-153,222,046 , GRCh37.p13 chr4: 154,143,198-154,143,198 TRIM2
    nsv5960043insertion1nstd209human GRCh38 chr4: 153,267,095-153,267,095 , GRCh37.p13 chr4: 154,188,247-154,188,247 TRIM2
    nsv5955349insertion1nstd209human GRCh38 chr4: 153,244,203-153,244,203 , GRCh37.p13 chr4: 154,165,355-154,165,355 TRIM2, LOC105377496
    nsv5906179copy number variation1nstd209human GRCh38 chr4: 153,208,425-153,208,568 , GRCh37.p13 chr4: 154,129,577-154,129,720 TRIM2
    nsv5905303copy number variation1nstd209human GRCh38 chr4: 153,314,170-153,314,438 , GRCh37.p13 chr4: 154,235,322-154,235,590 TRIM2
    nsv5895086copy number variation1nstd209human GRCh38 chr4: 153,318,479-153,321,878 , GRCh37.p13 chr4: 154,239,631-154,243,030 TRIM2
    nsv5838068copy number variation1nstd209human GRCh38 chr4: 153,318,419-153,321,868 , GRCh37.p13 chr4: 154,239,571-154,243,020 TRIM2
    nsv5728552mobile element insertion1nstd211human GRCh38 chr4: 153,265,289-153,265,289 , GRCh37.p13 chr4: 154,186,441-154,186,441 TRIM2, RNU6-1196P
    nsv5691930mobile element insertion2nstd211human GRCh38 chr4: 153,334,157-153,334,157 , GRCh37.p13 chr4: 154,255,309-154,255,309 TRIM2
    nsv5686189mobile element insertion2nstd211human GRCh38 chr4: 153,328,867-153,328,867 , GRCh37.p13 chr4: 154,250,019-154,250,019 TRIM2
    nsv5683866mobile element insertion1nstd211human GRCh38 chr4: 153,171,854-153,171,854 , GRCh37.p13 chr4: 154,093,006-154,093,006 TRIM2
    nsv5682493mobile element insertion1nstd211human GRCh38 chr4: 153,271,644-153,271,644 , GRCh37.p13 chr4: 154,192,796-154,192,796 TRIM2
    nsv5679571mobile element insertion1nstd211human GRCh38 chr4: 153,256,033-153,256,033 , GRCh37.p13 chr4: 154,177,185-154,177,185 TRIM2
    nsv5676241mobile element insertion2nstd211human GRCh38 chr4: 153,267,109-153,267,109 , GRCh37.p13 chr4: 154,188,261-154,188,261 TRIM2
    nsv5623861insertion1nstd207human GRCh38 chr4: 153,163,798-153,163,798 , GRCh37.p13 chr4: 154,084,950-154,084,950 TRIM2
    nsv5622189insertion1nstd207human GRCh38 chr4: 153,222,046-153,222,046 , GRCh37.p13 chr4: 154,143,198-154,143,198 TRIM2
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