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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5729332mobile element insertion1nstd211human GRCh38 chr17: 44,648,539-44,648,539 , GRCh37.p13 chr17: 42,725,907-42,725,907 LINC01180
    nsv5561825mobile element insertion1nstd206human GRCh38 chr17: 44,648,549-44,648,590 , GRCh37.p13 chr17: 42,725,917-42,725,958 LINC01180
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5016536copy number variation1nstd200human GRCh38 chr17: 44,648,169-44,648,804 , GRCh37.p13 chr17: 42,725,537-42,726,172 LINC01180
    nsv5013742copy number variation1nstd200human GRCh38 chr17: 44,647,594-44,653,333 , GRCh37.p13 chr17: 42,724,962-42,730,701 LINC01180
    nsv4867105copy number variation1nstd200human GRCh37 chr17: 42,725,537-42,726,172 , GRCh38.p12 chr17: 44,648,169-44,648,804 LINC01180
    nsv4632831copy number variation1nstd183human GRCh37 chr17: 42,668,792-42,774,693 , GRCh38.p12 chr17: 44,591,424-44,697,325 CCDC43, LINC01180, 3 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4261608copy number variation1nstd166human GRCh37.p13 chr17: 42,627,900-42,765,000 , GRCh38.p12 chr17: 44,550,532-44,687,632 FZD2, CCDC43, 4 more genes
    nsv4255824copy number variation1nstd166human GRCh37.p13 chr17: 42,721,184-42,722,647 , GRCh38.p12 chr17: 44,643,816-44,645,279 SMCO4P1, LINC01180
    nsv4253261copy number variation1nstd166human GRCh37.p13 chr17: 42,725,537-42,726,172 , GRCh38.p12 chr17: 44,648,169-44,648,804 LINC01180
    nsv3919609copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,648,246-42,839,745 , GRCh38 chr17: 43,570,878-44,762,377 , NCBI36 chr17: 39,003,772-40,195,271 SMCO4P1, LINC01180, 59 more genes
    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
    nsv3911344copy number variation1nstd102humanPathogenic GRCh37 chr17: 37,356,126-43,706,945 , NCBI36 chr17: 34,609,652-41,062,728 , GRCh38 chr17: 39,199,873-45,629,579 IFI35, RND2, 345 more genes
    nsv3910801copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,011,535-42,931,393 , GRCh38 chr17: 43,934,167-44,854,025 , NCBI36 chr17: 39,367,061-40,286,919 G6PC3, ITGA2B, 46 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 FOXK2, SOCS3-DT, 958 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
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