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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116876mobile element insertion1nstd186human GRCh37 chr2: 231,982,838-231,982,838 , GRCh38.p12 chr2: 231,118,124-231,118,124 PSMD1, HTR2B
    nsv5959112insertion1nstd209human GRCh38 chr2: 231,118,124-231,118,124 , GRCh37.p13 chr2: 231,982,838-231,982,838 PSMD1, HTR2B
    nsv5894046copy number variation1nstd209human GRCh38 chr2: 231,105,479-231,106,801 , GRCh37.p13 chr2: 231,970,193-231,971,515 HTR2B, PSMD1
    nsv5832543copy number variation1nstd209human GRCh38 chr2: 231,105,804-231,106,803 , GRCh37.p13 chr2: 231,970,518-231,971,517 PSMD1, HTR2B
    nsv5679775mobile element insertion2nstd211human GRCh38 chr2: 231,118,139-231,118,139 , GRCh37.p13 chr2: 231,982,853-231,982,853 PSMD1, HTR2B
    nsv5616061insertion1nstd207human GRCh38 chr2: 231,118,124-231,118,124 , GRCh37.p13 chr2: 231,982,838-231,982,838 PSMD1, HTR2B
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5436095copy number variation1nstd206human GRCh38 chr2: 231,118,287-231,118,382 , GRCh37.p13 chr2: 231,983,001-231,983,096 HTR2B, PSMD1
    nsv5400217mobile element insertion1nstd206human GRCh38 chr2: 231,118,124-231,118,124 , GRCh37.p13 chr2: 231,982,838-231,982,838 HTR2B, PSMD1
    nsv5351194translocation1nstd200human GRCh38 chr2: 231,105,480-231,105,480 , GRCh38 chr2: 231,106,802-231,106,802 , GRCh37.p13 chr2: 231,970,194-231,970,194 , GRCh37.p13 chr2: 231,971,516-231,971,516 HTR2B, PSMD1
    nsv5073982mobile element insertion1nstd203human GRCh38 chr2: 231,118,129-231,118,139 , GRCh37.p13 chr2: 231,982,843-231,982,853 HTR2B, PSMD1
    nsv5068591mobile element insertion1nstd203human GRCh38 chr2: 231,118,128-231,118,139 , GRCh37.p13 chr2: 231,982,842-231,982,853 PSMD1, HTR2B
    nsv5060970mobile element insertion1nstd203human GRCh38 chr2: 231,118,124-231,118,139 , GRCh37.p13 chr2: 231,982,838-231,982,853 PSMD1, HTR2B
    nsv4806238copy number variation1nstd200human GRCh37 chr2: 231,970,194-231,971,516 , GRCh38.p12 chr2: 231,105,480-231,106,802 HTR2B, PSMD1
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4724531insertion1nstd186human GRCh37 chr2: 231,982,838-231,982,838 , GRCh38.p12 chr2: 231,118,124-231,118,124 PSMD1, HTR2B
    nsv4686695mobile element insertion1nstd186human GRCh37 chr2: 231,982,853-231,982,853 , GRCh38.p12 chr2: 231,118,139-231,118,139 HTR2B, PSMD1
    nsv4679888copy number variation1nstd189human GRCh37.p13 chr2: 231,366,319-232,108,260 , GRCh38.p12 chr2: 230,501,604-231,243,547 HTR2B, PSMD1, 21 more genes
    nsv4673913copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,814,690-242,783,384 , GRCh38.p12 chr2: 229,949,974-241,841,232 MIR2467, D2HGDH, 270 more genes
    nsv4538016insertion1nstd166human GRCh37.p13 chr2: 231,982,838-231,982,838 , GRCh38.p12 chr2: 231,118,124-231,118,124 PSMD1, HTR2B
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