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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925384copy number variation1nstd209human GRCh38 chr8: 12,135,543-12,140,331 , GRCh37.p13 chr8: 11,993,052-11,997,840 USP17L2, FAM66D
    nsv5924248copy number variation1nstd209human GRCh38 chr8: 12,130,693-12,135,410 , GRCh37.p13 chr8: 11,988,202-11,992,919 USP17L2, USP17L7, 1 more genes
    nsv5857492copy number variation4nstd209human GRCh38 chr8: 12,135,342-12,137,718 , GRCh37.p13 chr8: 11,992,851-11,995,227 FAM66D, USP17L2
    nsv5849221copy number variation4nstd209human GRCh38 chr8: 12,135,343-12,139,627 , GRCh37.p13 chr8: 11,992,852-11,997,136 USP17L2, FAM66D
    nsv5671625inversion1nstd207human GRCh38 chr8: 7,301,025-12,600,730 , GRCh37.p13 chr8: 7,158,547-12,458,239 , BLK, 188 more genes
    nsv5419936copy number variation1nstd206human GRCh38 chr8: 12,130,647-12,135,424 , GRCh37.p13 chr8: 11,988,156-11,992,933 USP17L7, FAM66D, 1 more genes
    nsv5417141copy number variation1nstd206human GRCh38 chr8: 12,135,000-12,140,000 , GRCh37.p13 chr8: 11,992,509-11,997,509 FAM66D, USP17L2
    nsv5258635copy number variation1nstd204human GRCh38.p13 chr8: 12,137,518-12,151,171 , GRCh37.p13 chr8: 11,995,027-12,008,680 DEFB109D, FAM66D, 1 more genes
    nsv5257931copy number variation1nstd204human GRCh38.p13 chr8: 12,122,001-12,135,600 , GRCh37.p13 chr8: 11,979,510-11,993,109 LOC392196, USP17L2, 2 more genes
    nsv5256537copy number variation1nstd204human GRCh38.p13 chr8: 12,122,201-12,165,700 , GRCh37.p13 chr8: 11,979,710-12,023,209 USP17L7, USP17L2, 3 more genes
    nsv5255863copy number variation1nstd204human GRCh38.p13 chr8: 12,122,001-12,155,300 , GRCh37.p13 chr8: 11,979,510-12,012,809 LOC392196, FAM66D, 3 more genes
    nsv5253333copy number variation1nstd204human GRCh38.p13 chr8: 12,135,601-12,137,800 , GRCh37.p13 chr8: 11,993,110-11,995,309 USP17L2, FAM66D
    nsv5248193copy number variation1nstd204human GRCh38.p13 chr8: 12,123,201-12,155,300 , GRCh37.p13 chr8: 11,980,710-12,012,809 USP17L2, USP17L7, 3 more genes
    nsv5248043copy number variation1nstd204human GRCh38.p13 chr8: 12,135,201-12,140,000 , GRCh37.p13 chr8: 11,992,710-11,997,509 USP17L2, FAM66D
    nsv5246040copy number variation1nstd204human GRCh38.p13 chr8: 12,049,701-12,152,200 , GRCh37.p13 chr8: 11,907,210-12,009,709 ZNF705D, RNA5SP253, 8 more genes
    nsv5246015copy number variation1nstd204human GRCh38.p13 chr8: 12,137,501-12,139,700 , GRCh37.p13 chr8: 11,995,010-11,997,209 FAM66D, USP17L2
    nsv5244672copy number variation1nstd204human GRCh38.p13 chr8: 12,122,001-12,135,300 , GRCh37.p13 chr8: 11,979,510-11,992,809 USP17L2, USP17L7, 2 more genes
    nsv5244038copy number variation1nstd204human GRCh38.p13 chr8: 12,134,925-12,139,770 , GRCh37.p13 chr8: 11,992,434-11,997,279 USP17L2, FAM66D
    nsv5243511copy number variation1nstd204human GRCh38.p13 chr8: 12,122,548-12,135,341 , GRCh37.p13 chr8: 11,980,057-11,992,850 USP17L7, USP17L2, 2 more genes
    nsv5242673copy number variation1nstd204human GRCh38.p13 chr8: 12,129,201-12,140,100 , GRCh37.p13 chr8: 11,986,710-11,997,609 USP17L2, USP17L7, 2 more genes
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