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Items: 1 to 20 of 270

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965083insertion1nstd209human GRCh38 chr2: 201,414,934-201,414,934 , GRCh37.p13 chr2: 202,279,657-202,279,657 TRAK2
    nsv5897454copy number variation1nstd209human GRCh38 chr2: 201,221,824-201,490,725 , GRCh37.p13 chr2: 202,086,547-202,355,448 CASP8, CASP10, 5 more genes
    nsv5715026mobile element insertion1nstd211human GRCh38 chr2: 201,443,889-201,443,889 , GRCh37.p13 chr2: 202,308,612-202,308,612 TRAK2
    nsv5692914mobile element insertion1nstd211human GRCh38 chr2: 201,384,750-201,384,750 , GRCh37.p13 chr2: 202,249,473-202,249,473 TRAK2
    nsv5624043insertion1nstd207human GRCh38 chr2: 201,414,933-201,414,933 , GRCh37.p13 chr2: 202,279,656-202,279,656 TRAK2
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5434451copy number variation1nstd206human GRCh38 chr2: 201,449,296-201,453,100 , GRCh37.p13 chr2: 202,314,019-202,317,823 STRADB, TRAK2
    nsv5408255mobile element insertion1nstd206human GRCh38 chr2: 201,384,750-201,384,801 , GRCh37.p13 chr2: 202,249,473-202,249,524 TRAK2
    nsv5207191mobile element deletion1nstd204human GRCh38.p13 chr2: 201,424,576-201,424,911 , GRCh37.p13 chr2: 202,289,299-202,289,634 TRAK2
    nsv5199390mobile element insertion1nstd203human GRCh38 chr2: 201,443,872-201,443,889 , GRCh37.p13 chr2: 202,308,595-202,308,612 TRAK2
    nsv4910346copy number variation1nstd200human GRCh38 chr2: 201,441,469-201,447,210 , GRCh37.p13 chr2: 202,306,192-202,311,933 TRAK2
    nsv4910345copy number variation1nstd200human GRCh38 chr2: 201,415,440-201,415,587 , GRCh37.p13 chr2: 202,280,163-202,280,310 TRAK2
    nsv4910344copy number variation1nstd200human GRCh38 chr2: 201,386,540-201,386,678 , GRCh37.p13 chr2: 202,251,263-202,251,401 TRAK2
    nsv4910341copy number variation1nstd200human GRCh38 chr2: 201,342,198-201,398,768 , GRCh37.p13 chr2: 202,206,921-202,263,491 TRAK2, FLACC1
    nsv4795539copy number variation1nstd200human GRCh37 chr2: 202,206,921-202,263,491 , GRCh38.p12 chr2: 201,342,198-201,398,768 TRAK2, FLACC1
    nsv4777456mobile element deletion1nstd200human GRCh37 chr2: 202,289,309-202,289,629 , GRCh38.p12 chr2: 201,424,586-201,424,906 TRAK2
    nsv4760133insertion1nstd199human GRCh37 chr2: 202,279,654-202,279,654 , GRCh38.p12 chr2: 201,414,931-201,414,931 TRAK2
    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
    nsv4728199copy number variation1nstd102humanUncertain significance GRCh37 chr2: 202,011,822-202,749,788 , GRCh38.p12 chr2: 201,147,099-201,885,065 MTCO1P16, CFLAR, 26 more genes
    nsv4674597copy number variation1nstd102humanPathogenic GRCh37 chr2: 201,106,432-204,901,548 , GRCh38.p12 chr2: 200,241,709-204,036,825 KIAA2012-AS1, SNORD11, 113 more genes
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