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Items: 1 to 20 of 124

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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
    nsv7014917copy number variation1nstd229human GRCh38 chr19: 39,596,683-39,610,442 , GRCh37.p13 chr19: 40,087,323-40,101,082 RPS29P26, LGALS13
    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
    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
    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
    nsv5530252copy number variation1nstd206human GRCh38 chr19: 39,603,712-39,603,848 , GRCh37.p13 chr19: 40,094,352-40,094,488 LGALS13
    nsv4707508copy number variation1nstd195human GRCh38.p12 chr19: 39,530,511-39,628,061 , GRCh37 chr19: 40,021,151-40,118,701 LGALS13, EID2B, 6 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4423381copy number variation1nstd174human GRCh37 chr19: 40,081,716-40,188,788 , GRCh38.p12 chr19: 39,591,076-39,698,148 LGALS13, LGALS16, 6 more genes
    nsv4373090copy number variation1nstd173human GRCh37 chr19: 40,071,956-40,266,526 , GRCh38.p12 chr19: 39,581,316-39,775,886 LOC100129935, LGALS17A, 10 more genes
    nsv4270431copy number variation1nstd166human GRCh37.p13 chr19: 40,094,739-40,094,854 , GRCh38.p12 chr19: 39,604,099-39,604,214 LGALS13
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
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