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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140275copy number variation1nstd232human GRCh37.p13 chr19: 41,086,556-41,086,644 , GRCh38.p12 chr19: 40,580,650-40,580,738 SHKBP1
    nsv7139415copy number variation1nstd232human GRCh37.p13 chr19: 41,086,389-41,086,468 , GRCh38.p12 chr19: 40,580,483-40,580,562 SHKBP1
    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
    nsv7095278copy number variation1nstd102humanUncertain significance GRCh37 chr19: 40,882,496-41,135,455 , GRCh38.p12 chr19: 40,376,589-40,629,550 HIPK4, PRX, 8 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
    nsv7009238copy number variation1nstd229human GRCh38 chr19: 40,591,547-40,595,532 , GRCh37.p13 chr19: 41,097,453-41,101,438 LTBP4, SHKBP1
    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
    nsv7005657copy number variation1nstd229human GRCh38 chr19: 40,541,952-40,580,031 , GRCh37.p13 chr19: 41,047,858-41,085,937 SHKBP1, SPTBN4
    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
    nsv6624869copy number variation1nstd224human GRCh37 chr19: 41,084,106-41,187,337 , GRCh38.p12 chr19: 40,578,200-40,681,432 NUMBL, LTBP4, 1 more genes
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6521856copy number variation1nstd223human GRCh38 chr19: 40,577,481-40,579,459 , GRCh37.p13 chr19: 41,083,387-41,085,365 SHKBP1
    nsv6520332copy number variation1nstd223human GRCh38 chr19: 40,541,952-40,580,031 , GRCh37.p13 chr19: 41,047,858-41,085,937 SHKBP1, SPTBN4
    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
    nsv6251047mobile element insertion1nstd215human GRCh38 chr19: 40,583,183-40,583,183 , GRCh37.p13 chr19: 41,089,089-41,089,089 SHKBP1
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6101107insertion1nstd212human GRCh38 chr19: 40,583,170-40,583,170 , GRCh37.p13 chr19: 41,089,076-41,089,076 SHKBP1
    nsv5698062mobile element insertion2nstd211human GRCh38 chr19: 40,583,183-40,583,183 , GRCh37.p13 chr19: 41,089,089-41,089,089 SHKBP1
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