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Items: 1 to 20 of 511

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098420copy number variation1nstd102humanUncertain significance GRCh37 chr9: 117,046,993-117,072,977 , GRCh38.p12 chr9: 114,284,713-114,310,697 COL27A1, LOC105376224
    nsv7098419copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,917,341-116,918,270 , GRCh38.p12 chr9: 114,155,061-114,155,990 COL27A1
    nsv7098050copy number variation1nstd102humanUncertain significance GRCh37 chr9: 117,037,921-117,072,975 , GRCh38.p12 chr9: 114,275,641-114,310,695 LOC105376224, COL27A1
    nsv7098049copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,037,910-116,993,432 , GRCh38.p12 chr9: 113,275,630-114,231,152 POLE3, LOC100132609, 20 more genes
    nsv7097683copy number variation1nstd102humanUncertain significance GRCh37 chr9: 117,050,715-117,072,975 , GRCh38.p12 chr9: 114,288,435-114,310,695 COL27A1, LOC105376224
    nsv7069496inversion1nstd229human GRCh38 chr9: 114,106,457-114,343,346 , GRCh37.p13 chr9: 116,868,737-117,105,626 LOC105376224, ORM2, 5 more genes
    nsv7063963inversion1nstd229human GRCh38 chr9: 114,283,760-114,360,263 , GRCh37.p13 chr9: 117,046,040-117,122,543 LOC105376224, ORM2, 3 more genes
    nsv7058194inversion1nstd229human GRCh38 chr9: 114,053,312-114,284,714 , GRCh37.p13 chr9: 116,815,592-117,046,994 ZNF618, MIR455, 5 more genes
    nsv6877924copy number variation1nstd229human GRCh38 chr9: 114,183,327-114,185,596 , GRCh37.p13 chr9: 116,945,607-116,947,876 COL27A1
    nsv6876271copy number variation1nstd229human GRCh38 chr9: 114,266,422-114,266,566 , GRCh37.p13 chr9: 117,028,702-117,028,846 COL27A1
    nsv6873741copy number variation1nstd229human GRCh38 chr9: 114,106,491-114,284,713 , GRCh37.p13 chr9: 116,868,771-117,046,993 MIR455, LOC105376225, 1 more genes
    nsv6873701copy number variation1nstd229human GRCh38 chr9: 114,149,645-114,153,675 , GRCh37.p13 chr9: 116,911,925-116,915,955 LOC105376225, COL27A1
    nsv6871952copy number variation1nstd229human GRCh38 chr9: 114,173,214-114,173,453 , GRCh37.p13 chr9: 116,935,494-116,935,733 COL27A1
    nsv6871268copy number variation1nstd229human GRCh38 chr9: 114,237,199-114,237,380 , GRCh37.p13 chr9: 116,999,479-116,999,660 COL27A1
    nsv6868889copy number variation1nstd229human GRCh38 chr9: 114,155,093-114,155,120 , GRCh37.p13 chr9: 116,917,373-116,917,400 COL27A1
    nsv6868361copy number variation1nstd229human GRCh38 chr9: 114,216,063-114,219,503 , GRCh37.p13 chr9: 116,978,343-116,981,783 COL27A1
    nsv6867753copy number variation1nstd229human GRCh38 chr9: 114,206,498-114,206,700 , GRCh37.p13 chr9: 116,968,778-116,968,980 COL27A1
    nsv6866757copy number variation1nstd229human GRCh38 chr9: 114,193,158-114,371,753 , GRCh37.p13 chr9: 116,955,438-117,134,033 AKNA, COL27A1, 4 more genes
    nsv6866499copy number variation1nstd229human GRCh38 chr9: 114,281,113-114,381,248 , GRCh37.p13 chr9: 117,043,393-117,143,528 COL27A1, ORM1, 3 more genes
    nsv6865862copy number variation1nstd229human GRCh38 chr9: 114,255,710-114,260,823 , GRCh37.p13 chr9: 117,017,990-117,023,103 COL27A1
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