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Items: 1 to 20 of 151

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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
    nsv5323702copy number variation1nstd204human GRCh38.p13 chr17: 63,482,081-63,511,487 , GRCh37.p13 chr17: 61,559,442-61,588,848 ACE3P, ACE
    nsv5291986copy number variation1nstd204human GRCh38.p13 chr17: 63,481,627-63,510,087 , GRCh37.p13 chr17: 61,558,988-61,587,448 ACE3P, ACE
    nsv5013911copy number variation1nstd200human GRCh38 chr17: 63,490,897-63,532,417 , GRCh37.p13 chr17: 61,568,258-61,609,778 ACE, KCNH6, 1 more genes
    nsv4864767copy number variation1nstd200human GRCh37 chr17: 61,568,258-61,609,778 , GRCh38.p12 chr17: 63,490,897-63,532,417 ACE, ACE3P, 1 more genes
    nsv4864766copy number variation1nstd200human GRCh37 chr17: 61,559,451-61,588,840 , GRCh38.p12 chr17: 63,482,090-63,511,479 ACE, ACE3P
    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
    nsv4337198sequence alteration1nstd166human GRCh37.p13 chr17: 61,364,902-61,792,382 , GRCh38.p12 chr17: 63,287,541-63,715,022 , MAP3K3, 19 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
    nsv4270392copy number variation1nstd166human GRCh37.p13 chr17: 61,596,709-61,603,742 , GRCh38.p12 chr17: 63,519,348-63,526,381 ACE3P, KCNH6
    nsv4268952copy number variation1nstd166human GRCh37.p13 chr17: 61,582,390-61,582,459 , GRCh38.p12 chr17: 63,505,029-63,505,098 ACE3P
    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
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3904909copy number variation1nstd102humanPathogenic GRCh37 chr17: 59,597,348-64,886,364 , GRCh38.p12 chr17: 61,519,987-66,890,247 PRELID3BP3, PRKCA-AS1, 122 more genes
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