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Items: 1 to 20 of 260

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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
    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
    nsv7017128copy number variation1nstd229human GRCh38 chr19: 41,486,813-41,492,808 , GRCh37.p13 chr19|NW_004775434.1: 55,852-61,847 PCAT19
    nsv7014375copy number variation1nstd229human GRCh38 chr19: 41,464,201-41,502,300 , GRCh37.p13 chr19|NW_004775434.1: 33,240-71,339 PCAT19
    nsv7013879copy number variation1nstd229human GRCh38 chr19: 41,500,601-41,501,800 , GRCh37.p13 chr19|NW_004775434.1: 69,640-70,839 PCAT19
    nsv7011815copy number variation1nstd229human GRCh38 chr19: 41,450,865-41,455,675 , GRCh37.p13 chr19: 41,956,770-41,961,580 , GRCh37.p13 chr19|NW_004775434.1: 19,904-24,714 PCAT19, LOC107985329
    nsv7010457copy number variation1nstd229human GRCh38 chr19: 41,471,462-41,478,581 , GRCh37.p13 chr19|NW_004775434.1: 40,501-47,620 PCAT19
    nsv7008614copy number variation1nstd229human GRCh38 chr19: 41,464,181-41,516,791 , GRCh37.p13 chr19|NW_004775434.1: 33,220-85,830 TPM3P5, PCAT19
    nsv7008158copy number variation1nstd229human GRCh38 chr19: 41,494,910-41,521,625 , GRCh37.p13 chr19|NW_004775434.1: 63,949-90,664 PCAT19, PLEKHA3P1, 1 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
    nsv7006219copy number variation1nstd229human GRCh38 chr19: 41,456,701-41,460,900 , GRCh37.p13 chr19|NW_004775434.1: 25,740-29,939 PCAT19
    nsv7003948copy number variation1nstd229human GRCh38 chr19: 41,495,034-41,496,997 , GRCh37.p13 chr19|NW_004775434.1: 64,073-66,036 PCAT19
    nsv7003490copy number variation1nstd229human GRCh38 chr19: 41,464,501-41,503,500 , GRCh37.p13 chr19|NW_004775434.1: 33,540-72,539 PCAT19
    nsv7003274copy number variation1nstd229human GRCh38 chr19: 41,496,719-41,504,693 , GRCh37.p13 chr19|NW_004775434.1: 65,758-73,732 TPM3P5, PCAT19
    nsv7002572copy number variation1nstd229human GRCh38 chr19: 41,462,306-41,549,520 , GRCh37.p13 chr19|NW_004775434.1: 31,345-118,559 CEACAM21, PCAT19, 3 more genes
    nsv7002487copy number variation1nstd229human GRCh38 chr19: 41,464,064-41,516,961 , GRCh37.p13 chr19|NW_004775434.1: 33,103-86,000 PCAT19, TPM3P5
    nsv7001512copy number variation1nstd229human GRCh38 chr19: 41,466,701-41,503,500 , GRCh37.p13 chr19|NW_004775434.1: 35,740-72,539 PCAT19
    nsv7000175copy number variation1nstd229human GRCh38 chr19: 41,457,246-41,457,329 , GRCh37.p13 chr19|NW_004775434.1: 26,285-26,368 PCAT19
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