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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv5961615insertion1nstd209human GRCh38 chr2: 37,347,165-37,347,165 , GRCh37.p13 chr2: 37,574,308-37,574,308 QPCT
    nsv5951963insertion1nstd209human GRCh38 chr2: 37,343,662-37,343,662 , GRCh37.p13 chr2: 37,570,805-37,570,805 QPCT
    nsv5730521mobile element insertion1nstd211human GRCh38 chr2: 37,356,343-37,356,343 , GRCh37.p13 chr2: 37,583,486-37,583,486 QPCT
    nsv5680446mobile element insertion2nstd211human GRCh38 chr2: 37,359,200-37,359,200 , GRCh37.p13 chr2: 37,586,343-37,586,343 QPCT
    nsv5676250mobile element insertion2nstd211human GRCh38 chr2: 37,371,590-37,371,590 , GRCh37.p13 chr2: 37,598,733-37,598,733 QPCT
    nsv5623641insertion1nstd207human GRCh38 chr2: 37,347,200-37,347,200 , GRCh37.p13 chr2: 37,574,343-37,574,343 QPCT
    nsv5621587insertion1nstd207human GRCh38 chr2: 37,347,235-37,347,235 , GRCh37.p13 chr2: 37,574,378-37,574,378 QPCT
    nsv5406109mobile element insertion1nstd206human GRCh38 chr2: 37,359,200-37,359,251 , GRCh37.p13 chr2: 37,586,343-37,586,394 QPCT
    nsv5405214mobile element insertion1nstd206human GRCh38 chr2: 37,371,590-37,371,641 , GRCh37.p13 chr2: 37,598,733-37,598,784 QPCT
    nsv5199949mobile element insertion1nstd203human GRCh38 chr2: 37,356,327-37,356,343 , GRCh37.p13 chr2: 37,583,470-37,583,486 QPCT
    nsv5187245mobile element insertion1nstd203human GRCh38 chr2: 37,356,329-37,356,343 , GRCh37.p13 chr2: 37,583,472-37,583,486 QPCT
    nsv5069948mobile element insertion1nstd203human GRCh38 chr2: 37,359,194-37,359,200 , GRCh37.p13 chr2: 37,586,337-37,586,343 QPCT
    nsv4764802insertion1nstd199human GRCh37 chr2: 37,574,317-37,574,317 , GRCh38.p12 chr2: 37,347,174-37,347,174 QPCT
    nsv4728619copy number variation1nstd102humanUncertain significance GRCh37 chr2: 36,432,453-38,182,274 , GRCh38.p12 chr2: 36,205,310-37,955,131 CDC42EP3, NDUFAF7, 30 more genes
    nsv4585865copy number variation1nstd183human GRCh37 chr2: 37,479,579-37,742,813 , GRCh38.p12 chr2: 37,252,436-37,515,670 PRKD3, QPCT, 6 more genes
    nsv4534361insertion1nstd166human GRCh37.p13 chr2: 37,583,470-37,583,470 , GRCh38.p12 chr2: 37,356,327-37,356,327 QPCT
    nsv4466499mobile element insertion1nstd166human GRCh37.p13 chr2: 37,598,721-37,598,721 , GRCh38.p12 chr2: 37,371,578-37,371,578 QPCT
    nsv4466498mobile element insertion1nstd166human GRCh37.p13 chr2: 37,586,337-37,586,337 , GRCh38.p12 chr2: 37,359,194-37,359,194 QPCT
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