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Items: 1 to 20 of 173

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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
    nsv7008627copy number variation1nstd229human GRCh38 chr19: 39,364,901-39,554,300 , GRCh37.p13 chr19: 39,855,541-40,044,940 CRIPTOP7, ZFP36, 16 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
    nsv7007016copy number variation1nstd229human GRCh38 chr19: 39,516,972-39,517,134 , GRCh37.p13 chr19: 40,007,612-40,007,774 SELENOV
    nsv7006517copy number variation1nstd229human GRCh38 chr19: 39,517,058-39,536,626 , GRCh37.p13 chr19: 40,007,698-40,027,266 SELENOV, EID2B, 1 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
    nsv6624896copy number variation1nstd224human GRCh37 chr19: 39,989,922-40,009,683 , GRCh38.p12 chr19: 39,499,282-39,519,043 DLL3, SELENOV
    nsv6624713copy number variation1nstd224human GRCh37 chr19: 39,978,809-40,009,466 , GRCh38.p12 chr19: 39,488,169-39,518,826 DLL3, SELENOV, 1 more genes
    nsv6532198copy number variation1nstd223human GRCh38 chr19: 39,519,974-39,528,226 , GRCh37.p13 chr19: 40,010,614-40,018,866 SELENOV
    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
    nsv6110133insertion1nstd212human GRCh38 chr19: 39,517,063-39,517,063 , GRCh37.p13 chr19: 40,007,703-40,007,703 SELENOV
    nsv6057920copy number variation1nstd212human GRCh38 chr19: 39,515,154-39,517,367 , GRCh37.p13 chr19: 40,005,794-40,008,007 SELENOV
    nsv5719001mobile element insertion2nstd211human GRCh38 chr19: 39,517,078-39,517,078 , GRCh37.p13 chr19: 40,007,718-40,007,718 SELENOV
    nsv5557779mobile element insertion1nstd206human GRCh38 chr19: 39,517,078-39,517,129 , GRCh37.p13 chr19: 40,007,718-40,007,769 SELENOV
    nsv5521388copy number variation1nstd206human GRCh38 chr19: 39,517,706-39,518,040 , GRCh37.p13 chr19: 40,008,346-40,008,680 SELENOV
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