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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095480copy number variation4nstd102humanUncertain significance GRCh37 chr19: 39,904,727-42,931,301 , GRCh38.p12 chr19: 39,414,087-42,427,149 CYP2B6, EID2B, 140 more genes
    nsv7095205copy number variation2nstd102humanUncertain significance GRCh37 chr19: 39,205,089-40,913,839 , GRCh38.p12 chr19: 38,714,449-40,407,932 CCNP, NFKBIB, 81 more genes
    nsv7071361inversion1nstd229human GRCh38 chr19: 39,004,066-42,402,005 , GRCh37.p13 chr19: 39,494,706-42,906,157 RAB4B, RABAC1, 160 more genes
    nsv7068288inversion1nstd229human GRCh38 chr19: 39,023,970-42,945,419 , GRCh37.p13 chr19: 39,514,610-43,449,571 MIR4530, RNU6-195P, 178 more genes
    nsv7017828copy number variation1nstd229human GRCh38 chr19: 39,637,056-39,820,845 , GRCh37.p13 chr19: 40,127,696-40,311,485 CLC, LGALS14, 6 more genes
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7007120copy number variation1nstd229human GRCh38 chr19: 39,511,623-39,657,771 , GRCh37.p13 chr19: 40,002,263-40,148,411 LGALS13, LGALS16, 10 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7001742copy number variation1nstd229human GRCh38 chr19: 39,637,402-39,637,505 , GRCh37.p13 chr19: 40,128,042-40,128,145 LOC100129935
    nsv6530819copy number variation1nstd223human GRCh38 chr19: 39,636,101-39,636,900 , GRCh37.p13 chr19: 40,126,741-40,127,540 LOC100129935
    nsv6527023copy number variation1nstd223human GRCh38 chr19: 39,556,174-39,743,171 , GRCh37.p13 chr19: 40,046,814-40,233,811 LGALS14, LGALS16, 10 more genes
    nsv6522662copy number variation1nstd223human GRCh38 chr19: 39,637,056-39,820,842 , GRCh37.p13 chr19: 40,127,696-40,311,482 CLC, LGALS14, 6 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5947536copy number variation1nstd209human GRCh38 chr19: 39,637,402-39,637,504 , GRCh37.p13 chr19: 40,128,042-40,128,144 LOC100129935
    nsv5708222mobile element insertion1nstd211human GRCh38 chr19: 39,641,307-39,641,307 , GRCh37.p13 chr19: 40,131,947-40,131,947 LOC100129935
    nsv5515664copy number variation1nstd206human GRCh38 chr19: 39,637,402-39,637,509 , GRCh37.p13 chr19: 40,128,042-40,128,149 LOC100129935
    nsv5422420mobile element insertion1nstd206human GRCh38 chr19: 39,641,307-39,641,358 , GRCh37.p13 chr19: 40,131,947-40,131,998 LOC100129935
    nsv5027957copy number variation1nstd200human GRCh38 chr19: 39,637,056-39,820,842 , GRCh37.p13 chr19: 40,127,696-40,311,482 CLC, LGALS14, 6 more genes
    nsv4711595copy number variation1nstd195human GRCh37 chr19: 40,126,601-40,141,001 , GRCh38.p12 chr19: 39,635,961-39,650,361 LOC100129935, RPS29P30
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