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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980057insertion1nstd209human GRCh38 chr11: 14,478,464-14,478,464 , GRCh37.p13 chr11: 14,500,010-14,500,010 COPB1, RNU7-49P
    nsv5918703copy number variation1nstd209human GRCh38 chr11: 14,492,481-14,492,614 , GRCh37.p13 chr11: 14,514,027-14,514,160 COPB1
    nsv5705648mobile element insertion2nstd211human GRCh38 chr11: 14,478,481-14,478,481 , GRCh37.p13 chr11: 14,500,027-14,500,027 COPB1, RNU7-49P
    nsv5663303insertion1nstd207human GRCh38 chr11: 14,478,464-14,478,464 , GRCh37.p13 chr11: 14,500,010-14,500,010 RNU7-49P, COPB1
    nsv5512672copy number variation1nstd206human GRCh38 chr11: 14,477,109-14,478,469 , GRCh37.p13 chr11: 14,498,655-14,500,015 COPB1, RNU7-49P
    nsv5398164mobile element insertion1nstd206human GRCh38 chr11: 14,478,464-14,478,464 , GRCh37.p13 chr11: 14,500,010-14,500,010 RNU7-49P, COPB1
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5354762translocation1nstd200human GRCh38 chr11: 14,478,469-14,478,469 , GRCh38 chr11: 14,477,109-14,477,109 , GRCh37.p13 chr11: 14,500,015-14,500,015 , GRCh37.p13 chr11: 14,498,655-14,498,655 RNU7-49P, COPB1
    nsv5137058mobile element insertion1nstd203human GRCh38 chr11: 14,477,389-14,477,405 , GRCh37.p13 chr11: 14,498,935-14,498,951 RNU7-49P, COPB1
    nsv5136716mobile element insertion1nstd203human GRCh38 chr11: 14,477,353-14,477,389 , GRCh37.p13 chr11: 14,498,899-14,498,935 RNU7-49P, COPB1
    nsv5136020mobile element insertion1nstd203human GRCh38 chr11: 14,478,471-14,478,481 , GRCh37.p13 chr11: 14,500,017-14,500,027 COPB1, RNU7-49P
    nsv5135430mobile element insertion1nstd203human GRCh38 chr11: 14,478,465-14,478,481 , GRCh37.p13 chr11: 14,500,011-14,500,027 RNU7-49P, COPB1
    nsv5134630mobile element insertion1nstd203human GRCh38 chr11: 14,478,468-14,478,481 , GRCh37.p13 chr11: 14,500,014-14,500,027 RNU7-49P, COPB1
    nsv5134486mobile element insertion1nstd203human GRCh38 chr11: 14,478,656-14,478,656 , GRCh37.p13 chr11: 14,500,202-14,500,202 COPB1, RNU7-49P
    nsv5133251mobile element insertion1nstd203human GRCh38 chr11: 14,478,703-14,478,703 , GRCh37.p13 chr11: 14,500,249-14,500,249 COPB1, RNU7-49P
    nsv5132304mobile element insertion1nstd203human GRCh38 chr11: 14,478,463-14,478,463 , GRCh37.p13 chr11: 14,500,009-14,500,009 COPB1, RNU7-49P
    nsv5128783mobile element insertion1nstd203human GRCh38 chr11: 14,478,698-14,478,698 , GRCh37.p13 chr11: 14,500,244-14,500,244 COPB1, RNU7-49P
    nsv5128269mobile element insertion1nstd203human GRCh38 chr11: 14,478,464-14,478,481 , GRCh37.p13 chr11: 14,500,010-14,500,027 RNU7-49P, COPB1
    nsv5127709mobile element insertion1nstd203human GRCh38 chr11: 14,477,387-14,477,389 , GRCh37.p13 chr11: 14,498,933-14,498,935 RNU7-49P, COPB1
    nsv5122753mobile element insertion1nstd203human GRCh38 chr11: 14,478,469-14,478,481 , GRCh37.p13 chr11: 14,500,015-14,500,027 RNU7-49P, COPB1
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