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Items: 1 to 20 of 184

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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
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7009879copy number variation1nstd229human GRCh38 chr19: 40,204,427-40,204,597 , GRCh37.p13 chr19: 40,710,334-40,710,504 MAP3K10
    nsv7008831copy number variation1nstd229human GRCh38 chr19: 40,208,566-40,243,653 , GRCh37.p13 chr19: 40,714,473-40,749,560 CCNP, TTC9B, 2 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
    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
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6598343inversion1nstd223human GRCh38 chr19: 40,206,822-40,207,566 , GRCh37.p13 chr19: 40,712,729-40,713,473 MAP3K10
    nsv6524387copy number variation1nstd223human GRCh38 chr19: 40,195,782-40,197,523 , GRCh37.p13 chr19: 40,701,689-40,703,430 MAP3K10
    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
    nsv5947050copy number variation1nstd209human GRCh38 chr19: 40,195,435-40,195,511 , GRCh37.p13 chr19: 40,701,342-40,701,418 MAP3K10
    nsv5720446mobile element insertion1nstd211human GRCh38 chr19: 40,215,623-40,215,623 , GRCh37.p13 chr19: 40,721,530-40,721,530 MAP3K10, TTC9B
    nsv5558284sequence alteration1nstd206human GRCh38 chr19: 40,171,920-40,325,062 , GRCh37.p13 chr19: 40,677,827-40,830,969 AKT2, MAP3K10, 6 more genes
    nsv5518448copy number variation1nstd206human GRCh38 chr19: 40,198,806-40,199,924 , GRCh37.p13 chr19: 40,704,713-40,705,831 MAP3K10
    nsv5375439translocation1nstd200human GRCh38 chr19: 40,207,337-40,207,337 , GRCh38 chr19: 40,206,826-40,206,826 , GRCh37.p13 chr19: 40,713,244-40,713,244 , GRCh37.p13 chr19: 40,712,733-40,712,733 MAP3K10
    nsv5336292translocation1nstd200human GRCh37 chr19: 40,701,419-40,701,419 , GRCh37 chr19: 40,701,343-40,701,343 , GRCh38.p12 chr19: 40,195,512-40,195,512 , GRCh38.p12 chr19: 40,195,436-40,195,436 MAP3K10
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