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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5220358mobile element deletion1nstd204human GRCh37.p13 chr17|NW_003315947.1: 285,429-285,753 , GRCh37.p13 chr17: 62,477,699-62,478,023 , GRCh38.p13 chr17: 64,481,582-64,481,906 POLG2, MILR1
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv5010623copy number variation1nstd200human GRCh38 chr17: 64,493,690-64,495,850 , GRCh37.p13 chr17|NW_003315947.1: 297,537-299,697 , GRCh37.p13 chr17: 62,489,807-62,491,968 POLG2, MILR1
    nsv5010622copy number variation1nstd200human GRCh38 chr17: 64,493,034-64,495,998 , GRCh37.p13 chr17: 62,489,151-62,492,116 , GRCh37.p13 chr17|NW_003315947.1: 296,881-299,845 POLG2, MILR1
    nsv5010621copy number variation1nstd200human GRCh38 chr17: 64,477,089-64,477,203 , GRCh37.p13 chr17|NW_003315947.1: 280,936-281,050 , GRCh37.p13 chr17: 62,473,206-62,473,320 POLG2, MILR1
    nsv4851657copy number variation1nstd200human GRCh37 chr17: 62,489,151-62,492,117 , GRCh38.p12 chr17: 64,493,034-64,495,999 MILR1, POLG2
    nsv4851656copy number variation1nstd200human GRCh37 chr17: 62,473,206-62,473,320 , GRCh38.p12 chr17: 64,477,089-64,477,203 POLG2, MILR1
    nsv4769535mobile element deletion1nstd200human GRCh37 chr17: 62,477,708-62,478,015 , GRCh38.p12 chr17: 64,481,591-64,481,898 POLG2, MILR1
    nsv4457799copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,869,604-67,078,443 , GRCh38.p12 chr17: 59,792,243-69,082,302 PECAM1, TBX2-AS1, 215 more genes
    nsv4349383copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,357,088-66,306,668 , GRCh38.p12 chr17: 59,279,727-68,310,527 FAM136DP, HELZ, 214 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
    nsv4252953copy number variation1nstd166human GRCh37.p13 chr17: 62,482,452-62,482,955 , GRCh38.p12 chr17: 64,486,335-64,486,838 MILR1, POLG2
    nsv3922133copy number variation1nstd102humanUncertain significance GRCh38 chr17: 64,307,125-64,748,462 , GRCh37.p13 chr17|NW_003315947.1: 110,972-457,041 , NCBI36 chr17: 59,738,217-60,175,042 MICOS10P2, KPNA2P3, 12 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
    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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