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Items: 1 to 20 of 150

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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
    nsv7015166copy number variation1nstd229human GRCh38 chr19: 40,020,924-40,026,487 , GRCh37.p13 chr19: 40,526,831-40,532,394 LOC390933, ZNF546, 1 more genes
    nsv7012529copy number variation1nstd229human GRCh38 chr19: 40,025,138-40,030,124 , GRCh37.p13 chr19: 40,531,045-40,536,031 ZNF780B, LOC390933
    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
    nsv7000087copy number variation1nstd229human GRCh38 chr19: 39,937,301-40,261,900 , GRCh37.p13 chr19: 40,443,208-40,767,807 ZNF780A, CCNP, 10 more genes
    nsv6531375copy number variation1nstd223human GRCh38 chr19: 40,056,801-40,058,800 , GRCh37.p13 chr19: 40,562,708-40,564,707 ZNF780B
    nsv6526230copy number variation1nstd223human GRCh38 chr19: 40,039,395-40,041,989 , GRCh37.p13 chr19: 40,545,302-40,547,896 ZNF780B
    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
    nsv6133702copy number variation1nstd213human GRCh37 chr19: 40,470,000-40,680,001 , GRCh38.p12 chr19: 39,964,093-40,174,094 , GRCh38.p12 chr19|NW_009646206.1: 239,236-370,917 PSMC4, ZNF780B, 4 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
    nsv5931355copy number variation1nstd209human GRCh38 chr19: 40,034,424-40,034,674 , GRCh37.p13 chr19: 40,540,331-40,540,581 ZNF780B
    nsv5333417translocation1nstd200human GRCh37 chr19: 40,566,970-40,566,970 , GRCh37 chr19: 40,567,063-40,567,063 , GRCh38.p12 chr19|NW_009646206.1: 336,206-336,206 , GRCh38.p12 chr19: 40,061,156-40,061,156 , GRCh38.p12 chr19: 40,061,063-40,061,063 , GRCh38.p12 chr19|NW_009646206.1: 336,299-336,299 ZNF780B
    nsv5322256translocation1nstd204human GRCh38.p13 chr19: 40,061,156-40,061,156 , GRCh38.p13 chr19: 40,061,063-40,061,063 , GRCh37.p13 chr19: 40,567,063-40,567,063 , GRCh37.p13 chr19: 40,566,970-40,566,970 ZNF780B
    nsv5298756copy number variation1nstd204human GRCh38.p13 chr19: 40,040,261-40,042,498 , GRCh37.p13 chr19: 40,546,168-40,548,405 ZNF780B
    nsv5295387copy number variation1nstd204human GRCh38.p13 chr19: 40,049,986-40,054,469 , GRCh37.p13 chr19: 40,555,893-40,560,376 ZNF780B
    nsv5290896copy number variation1nstd204human GRCh38.p13 chr19: 40,050,001-40,054,600 , GRCh37.p13 chr19: 40,555,908-40,560,507 ZNF780B
    nsv5027981copy number variation1nstd200human GRCh38 chr19: 40,039,375-40,041,996 , GRCh37.p13 chr19: 40,545,282-40,547,903 ZNF780B
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