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Items: 1 to 20 of 158

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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
    nsv7075514inversion1nstd229human GRCh38 chr19: 38,994,526-39,502,034 , GRCh37.p13 chr19: 39,485,166-39,992,674 RPS16, PLEKHG2, 25 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
    nsv7006083copy number variation1nstd229human GRCh38 chr19: 39,416,710-39,419,294 , GRCh37.p13 chr19: 39,907,350-39,909,934 PLEKHG2
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 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
    nsv5944000copy number variation1nstd209human GRCh38 chr19: 39,387,653-39,412,021 , GRCh37.p13 chr19: 39,878,293-39,902,661 ZFP36, PAF1, 5 more genes
    nsv5662764insertion1nstd207human GRCh38 chr19: 39,413,589-39,413,589 , GRCh37.p13 chr19: 39,904,229-39,904,229 PLEKHG2
    nsv5528258copy number variation1nstd206human GRCh38 chr19: 39,409,499-39,412,022 , GRCh37.p13 chr19: 39,900,139-39,902,662 PLEKHG2, ZFP36, 2 more genes
    nsv4632480copy number variation2nstd183human GRCh37 chr19: 39,904,419-39,904,463 , GRCh38.p12 chr19: 39,413,779-39,413,823 PLEKHG2
    nsv4624865copy number variation1nstd183human GRCh37 chr19: 39,881,236-39,904,463 , GRCh38.p12 chr19: 39,390,596-39,413,823 ZFP36, PAF1, 5 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
    nsv4257080copy number variation1nstd166human GRCh37.p13 chr19: 39,918,698-39,922,161 , GRCh38.p12 chr19: 39,428,058-39,431,521 RPS16, PLEKHG2
    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
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