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Items: 1 to 20 of 454

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958996insertion1nstd209human GRCh38 chr2: 201,574,191-201,574,191 , GRCh37.p13 chr2: 202,438,914-202,438,914 C2CD6
    nsv5949632insertion1nstd209human GRCh38 chr2: 201,534,534-201,534,534 , GRCh37.p13 chr2: 202,399,257-202,399,257 C2CD6
    nsv5906872copy number variation1nstd209human GRCh38 chr2: 201,515,193-201,515,242 , GRCh37.p13 chr2: 202,379,916-202,379,965 C2CD6
    nsv5903702copy number variation1nstd209human GRCh38 chr2: 201,595,693-201,595,794 , GRCh37.p13 chr2: 202,460,416-202,460,517 C2CD6
    nsv5897696copy number variation1nstd209human GRCh38 chr2: 201,508,948-201,510,346 , GRCh37.p13 chr2: 202,373,671-202,375,069 C2CD6
    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
    nsv5832366copy number variation1nstd209human GRCh38 chr2: 201,508,907-201,510,341 , GRCh37.p13 chr2: 202,373,630-202,375,064 C2CD6
    nsv5727673mobile element insertion1nstd211human GRCh38 chr2: 201,595,208-201,595,208 , GRCh37.p13 chr2: 202,459,931-202,459,931 C2CD6
    nsv5726141mobile element insertion1nstd211human GRCh38 chr2: 201,491,915-201,491,915 , GRCh37.p13 chr2: 202,356,638-202,356,638 C2CD6
    nsv5716480mobile element insertion1nstd211human GRCh38 chr2: 201,567,223-201,567,223 , GRCh37.p13 chr2: 202,431,946-202,431,946 C2CD6
    nsv5692304mobile element insertion1nstd211human GRCh38 chr2: 201,595,906-201,595,906 , GRCh37.p13 chr2: 202,460,629-202,460,629 C2CD6
    nsv5689038mobile element insertion2nstd211human GRCh38 chr2: 201,572,338-201,572,338 , GRCh37.p13 chr2: 202,437,061-202,437,061 C2CD6
    nsv5685817mobile element insertion1nstd211human GRCh38 chr2: 201,521,095-201,521,095 , GRCh37.p13 chr2: 202,385,818-202,385,818 C2CD6
    nsv5680665mobile element insertion1nstd211human GRCh38 chr2: 201,502,908-201,502,908 , GRCh37.p13 chr2: 202,367,631-202,367,631 C2CD6
    nsv5676010mobile element insertion1nstd211human GRCh38 chr2: 201,601,295-201,601,295 , GRCh37.p13 chr2: 202,466,018-202,466,018 C2CD6
    nsv5674976mobile element insertion2nstd211human GRCh38 chr2: 201,574,206-201,574,206 , GRCh37.p13 chr2: 202,438,929-202,438,929 C2CD6
    nsv5673454copy number variation1nstd102humanPathogenic GRCh37 chr2: 202,466,462-202,508,123 , GRCh38.p12 chr2: 201,601,739-201,643,400 TMEM237, C2CD6, 2 more genes
    nsv5619859insertion1nstd207human GRCh38 chr2: 201,595,693-201,595,693 , GRCh37.p13 chr2: 202,460,416-202,460,416 C2CD6
    nsv5578014copy number variation1nstd207human GRCh38 chr2: 201,563,372-201,563,468 , GRCh37.p13 chr2: 202,428,095-202,428,191 C2CD6
    nsv5574026copy number variation1nstd207human GRCh38 chr2: 201,508,948-201,510,346 , GRCh37.p13 chr2: 202,373,671-202,375,069 C2CD6
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