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Items: 1 to 20 of 116

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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
    nsv7069067inversion1nstd229human GRCh38 chr19: 41,426,319-41,430,091 , GRCh37.p13 chr19: 41,932,224-41,935,996 DMAC2, B3GNT8
    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
    nsv7014693copy number variation1nstd229human GRCh38 chr19: 41,351,628-41,450,794 , GRCh37.p13 chr19: 41,857,533-41,936,866 DMAC2, TMEM91, 7 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
    nsv7004339copy number variation1nstd229human GRCh38 chr19: 41,411,829-41,432,986 , GRCh37.p13 chr19: 41,917,734-41,936,866 BCKDHA, DMAC2, 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
    nsv6535162copy number variation1nstd223human GRCh38 chr19: 41,351,628-41,450,794 , GRCh37.p13 chr19: 41,857,533-41,936,866 DMAC2, B3GNT8, 7 more genes
    nsv6310484copy number variation1nstd102humanPathogenic GRCh37 chr19: 41,925,030-41,930,736 , GRCh38.p12 chr19: 41,419,125-41,424,831 B3GNT8, BCKDHA
    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
    nsv5673236copy number variation1nstd102humanPathogenic GRCh37 chr19: 41,903,723-41,930,736 , GRCh38.p12 chr19: 41,397,818-41,424,831 BCKDHA, EXOSC5, 1 more genes
    nsv5520666copy number variation1nstd206human GRCh38 chr19: 41,417,746-41,423,703 , GRCh37.p13 chr19: 41,923,651-41,929,608 BCKDHA, B3GNT8
    nsv5288731copy number variation1nstd204human GRCh38.p13 chr19: 41,182,901-41,435,300 , GRCh37.p13 chr19: 41,688,806-41,936,866 LOC105372401, AXL, 13 more genes
    nsv5024653copy number variation1nstd200human GRCh38 chr19: 41,351,628-41,450,794 , GRCh37.p13 chr19: 41,857,533-41,936,866 BCKDHA, B9D2, 7 more genes
    nsv4865179copy number variation1nstd200human GRCh37 chr19: 41,857,533-41,956,699 , GRCh38.p12 chr19: 41,351,628-41,450,794 B9D2, BCKDHA, 7 more genes
    nsv4683302copy number variation1nstd102humanPathogenic GRCh37 chr19: 41,930,333-41,930,736 , GRCh38.p12 chr19: 41,424,428-41,424,831 BCKDHA, B3GNT8
    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
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