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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5886263copy number variation1nstd209human GRCh38 chr17: 42,959,180-42,960,579 , GRCh37.p13 chr17: 41,111,197-41,112,596 PTGES3L-AARSD1, AARSD1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5521948copy number variation1nstd206human GRCh38 chr17: 42,959,174-42,960,759 , GRCh37.p13 chr17: 41,111,191-41,112,776 AARSD1, PTGES3L-AARSD1
    nsv5287669copy number variation1nstd204human GRCh38.p13 chr17: 42,963,201-43,231,700 , GRCh37.p13 chr17: 41,115,218-41,383,489 PTGES3L, CCDC200, 15 more genes
    nsv5016455copy number variation1nstd200human GRCh38 chr17: 42,948,746-42,959,944 , GRCh37.p13 chr17: 41,100,763-41,111,961 PTGES3L-AARSD1, AARSD1
    nsv5016453copy number variation1nstd200human GRCh38 chr17: 42,944,758-42,948,782 , GRCh37.p13 chr17: 41,096,775-41,100,799 AARSD1, PTGES3L-AARSD1
    nsv5013721copy number variation1nstd200human GRCh38 chr17: 42,960,035-42,965,037 , GRCh37.p13 chr17: 41,112,052-41,117,054 AARSD1, PTGES3L-AARSD1
    nsv4867044copy number variation1nstd200human GRCh37 chr17: 41,111,222-41,112,685 , GRCh38.p12 chr17: 42,959,205-42,960,668 PTGES3L-AARSD1, AARSD1
    nsv4867043copy number variation1nstd200human GRCh37 chr17: 41,100,762-41,111,961 , GRCh38.p12 chr17: 42,948,745-42,959,944 PTGES3L-AARSD1, AARSD1
    nsv4864659copy number variation1nstd200human GRCh37 chr17: 41,112,043-41,117,061 , GRCh38.p12 chr17: 42,960,026-42,965,044 PTGES3L-AARSD1, AARSD1
    nsv4858858copy number variation1nstd200human GRCh37 chr17: 41,096,802-41,100,778 , GRCh38.p12 chr17: 42,944,785-42,948,761 PTGES3L-AARSD1, AARSD1
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4272232copy number variation1nstd166human GRCh37.p13 chr17: 41,116,712-41,117,445 , GRCh38.p12 chr17: 42,964,695-42,965,428 PTGES3L-AARSD1, AARSD1
    nsv4270582copy number variation1nstd166human GRCh37.p13 chr17: 41,100,762-41,111,961 , GRCh38.p12 chr17: 42,948,745-42,959,944 PTGES3L-AARSD1, AARSD1
    nsv4269113copy number variation1nstd166human GRCh37.p13 chr17: 41,102,956-41,103,247 , GRCh38.p12 chr17: 42,950,939-42,951,230 AARSD1, PTGES3L-AARSD1
    nsv4261992copy number variation1nstd166human GRCh37.p13 chr17: 41,112,000-41,117,000 , GRCh38.p12 chr17: 42,959,983-42,964,983 PTGES3L-AARSD1, AARSD1
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
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