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Items: 1 to 20 of 123

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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
    nsv7014801copy number variation1nstd229human GRCh38 chr19: 41,538,845-41,580,503 , GRCh37.p13 chr19|NW_004775434.1: 107,884-149,542 , GRCh37.p13 chr19: 42,050,111-42,086,856 CEACAM21, LOC110467527
    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
    nsv7002199copy number variation1nstd229human GRCh38 chr19: 41,564,852-41,571,954 , GRCh37.p13 chr19|NW_004775434.1: 133,891-140,993 , GRCh37.p13 chr19: 42,071,206-42,078,306 CEACAM21, LOC110467527
    nsv7002137copy number variation1nstd229human GRCh38 chr19: 41,550,866-41,670,985 , GRCh37.p13 chr19: 42,057,234-42,174,913 , GRCh37.p13 chr19|NW_004775434.1: 119,905-240,024 DNAJC19P2, LOC105372404, 6 more genes
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6525936copy number variation1nstd223human GRCh38 chr19: 41,564,852-41,571,949 , GRCh37.p13 chr19: 42,071,206-42,078,301 , GRCh37.p13 chr19|NW_004775434.1: 133,891-140,988 LOC110467527, CEACAM21
    nsv6517423copy number variation1nstd223human GRCh38 chr19: 41,550,866-41,670,990 , GRCh37.p13 chr19|NW_004775434.1: 119,905-240,029 , GRCh37.p13 chr19: 42,057,234-42,174,918 DNAJC19P2, LOC110467527, 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
    nsv5359806translocation1nstd200human GRCh38 chr19: 41,565,111-41,565,111 , GRCh38 chr19: 41,565,171-41,565,171 , GRCh37.p13 chr19|NW_004775434.1: 134,210-134,210 , GRCh37.p13 chr19: 42,071,465-42,071,465 , GRCh37.p13 chr19|NW_004775434.1: 134,150-134,150 , GRCh37.p13 chr19: 42,071,525-42,071,525 LOC110467527, CEACAM21
    nsv5024655copy number variation1nstd200human GRCh38 chr19: 41,550,866-41,670,990 , GRCh37.p13 chr19|NW_004775434.1: 119,905-240,029 , GRCh37.p13 chr19: 42,057,234-42,174,918 DNAJC19P3, LOC105372404, 6 more genes
    nsv4702641copy number variation1nstd195human GRCh37 chr19: 41,998,201-42,367,401 , GRCh38.p12 chr19: 41,492,293-41,863,329 , GRCh38.p12 chr19|NT_187620.1: 1-198,050 CEACAM5, CEACAM7, 20 more genes
    nsv4676231copy number variation1nstd102humanUncertain significance GRCh37 chr19: 41,889,319-42,338,832 , GRCh38.p12 chr19: 41,383,414-41,834,777 , GRCh38.p12 chr19|NT_187620.1: 1-233,762 CEACAM7, LYPD4, 25 more genes
    nsv4632159copy number variation1nstd183human GRCh37 chr19: 42,057,346-42,172,442 , GRCh38.p12 chr19: 41,550,978-41,668,514 , GRCh38.p12 chr19|NT_187620.1: 13,487-131,023 CEACAM4, CEACAMP3, 6 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
    nsv4267237copy number variation1nstd166human GRCh37.p13 chr19: 42,071,465-42,071,525 , GRCh38.p12 chr19|NT_187620.1: 116,830-116,890 , GRCh38.p12 chr19: 41,565,111-41,565,171 LOC110467527, CEACAM21
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