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Items: 1 to 20 of 721

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143558insertion1nstd232human GRCh37.p13 chr21: 44,135,843-44,135,843 , GRCh38.p12 chr21: 42,715,733-42,715,733 PDE9A
    nsv7096096copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr21: 43,160,998-47,754,702 , GRCh38.p12 chr21: 41,740,838-46,334,788 TSPEAR, LINC01424, 158 more genes
    nsv7076046inversion1nstd229human GRCh38 chr21: 42,633,367-44,550,173 , GRCh37.p13 chr21: 44,053,477-45,916,560 MYL6P1, MIR5692B, 68 more genes
    nsv7072799inversion1nstd229human GRCh38 chr21: 41,886,117-43,786,596 , GRCh37.p13 chr21: 43,306,226-45,206,477 ZNF295-AS1, LINC01668, 57 more genes
    nsv7064889inversion1nstd229human GRCh38 chr21: 41,632,756-44,900,321 , GRCh37.p13 chr21: 43,052,916-46,320,236 RNU6-1150P, LOC105372824, 123 more genes
    nsv7036183copy number variation1nstd229human GRCh38 chr21: 42,741,765-42,741,845 , GRCh37.p13 chr21: 44,161,875-44,161,955 PDE9A-AS1, PDE9A
    nsv7035632copy number variation1nstd229human GRCh38 chr21: 42,714,601-42,719,800 , GRCh37.p13 chr21: 44,134,711-44,139,910 PDE9A
    nsv7034050copy number variation1nstd229human GRCh38 chr21: 42,705,801-42,711,300 , GRCh37.p13 chr21: 44,125,911-44,131,410 PDE9A
    nsv7033523copy number variation1nstd229human GRCh38 chr21: 42,761,823-42,809,798 , GRCh37.p13 chr21: 44,181,933-44,229,908 PDE9A, LINC01668, 1 more genes
    nsv7031766copy number variation1nstd229human GRCh38 chr21: 42,679,602-42,679,766 , GRCh37.p13 chr21: 44,099,712-44,099,876 PDE9A
    nsv7031528copy number variation1nstd229human GRCh38 chr21: 42,704,701-42,711,300 , GRCh37.p13 chr21: 44,124,811-44,131,410 PDE9A
    nsv7027664copy number variation1nstd229human GRCh38 chr21: 42,655,110-42,656,678 , GRCh37.p13 chr21: 44,075,220-44,076,788 PDE9A
    nsv7027215copy number variation1nstd229human GRCh38 chr21: 42,689,832-42,697,797 , GRCh37.p13 chr21: 44,109,942-44,117,907 PDE9A
    nsv7027011copy number variation1nstd229human GRCh38 chr21: 42,282,878-43,017,165 , GRCh37.p13 chr21: 43,702,988-44,437,275 LOC105372817, RNU6-1149P, 23 more genes
    nsv7026785copy number variation1nstd229human GRCh38 chr21: 42,690,583-42,693,124 , GRCh37.p13 chr21: 44,110,693-44,113,234 PDE9A
    nsv7026212copy number variation1nstd229human GRCh38 chr21: 42,615,301-42,698,300 , GRCh37.p13 chr21: 44,035,411-44,118,410 LOC101928255, PDE9A, 1 more genes
    nsv7026189copy number variation1nstd229human GRCh38 chr21: 42,662,328-42,665,010 , GRCh37.p13 chr21: 44,082,438-44,085,120 PDE9A
    nsv7025882copy number variation1nstd229human GRCh38 chr21: 42,715,445-42,719,681 , GRCh37.p13 chr21: 44,135,555-44,139,791 PDE9A
    nsv7025533copy number variation1nstd229human GRCh38 chr21: 42,683,854-42,687,283 , GRCh37.p13 chr21: 44,103,964-44,107,393 PDE9A
    nsv7024099copy number variation1nstd229human GRCh38 chr21: 41,989,601-42,863,900 , GRCh37.p13 chr21: 43,409,710-44,284,010 PDE9A, RNA5SP492, 25 more genes
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