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Items: 1 to 20 of 222

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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
    nsv7095280copy number variation1nstd102humanUncertain significance GRCh37 chr19: 41,201,874-41,201,979 , GRCh38.p12 chr19: 40,695,969-40,696,074 COQ8B
    nsv7095208copy number variation1nstd102humanUncertain significance GRCh37 chr19: 41,114,106-41,201,979 , GRCh38.p12 chr19: 40,608,200-40,696,074 LTBP4, NUMBL, 1 more genes
    nsv7071458inversion1nstd229human GRCh38 chr19: 40,692,526-40,695,704 , GRCh37.p13 chr19: 41,198,431-41,201,609 COQ8B
    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
    nsv7016735copy number variation1nstd229human GRCh38 chr19: 40,681,401-40,728,800 , GRCh37.p13 chr19: 41,187,306-41,234,705 NUMBL, RNU6-195P, 2 more genes
    nsv7010872copy number variation1nstd229human GRCh38 chr19: 40,713,231-40,733,810 , GRCh37.p13 chr19: 41,219,136-41,239,715 COQ8B, ITPKC
    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
    nsv7002183copy number variation1nstd229human GRCh38 chr19: 40,225,202-40,756,025 , GRCh37.p13 chr19: 40,731,109-41,261,930 RNU6-195P, LTBP4, 21 more genes
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6530745copy number variation1nstd223human GRCh38 chr19: 40,695,084-40,698,076 , GRCh37.p13 chr19: 41,200,989-41,203,981 COQ8B
    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
    nsv6285102insertion1nstd214human GRCh38 chr19: 40,702,821-40,702,821 , GRCh37.p13 chr19: 41,208,726-41,208,726 COQ8B
    nsv6144971copy number variation1nstd206human GRCh38 chr19: 40,708,874-40,776,874 , GRCh37.p13 chr19: 41,214,779-41,282,779 SNRPA, MIA, 6 more genes
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 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
    nsv6130770insertion1nstd186human GRCh37 chr19: 41,219,587-41,219,607 , GRCh38.p12 chr19: 40,713,682-40,713,702 COQ8B
    nsv6128315copy number variation1nstd186human GRCh37 chr19: 41,208,726-41,208,801 , GRCh38.p12 chr19: 40,702,821-40,702,896 COQ8B
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