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Items: 1 to 20 of 156

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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
    nsv5520511copy number variation1nstd206human GRCh38 chr17: 64,526,861-64,526,920 , GRCh37.p13 chr17: 62,522,979-62,523,038 , GRCh37.p13 chr17|NW_003315947.1: 330,708-330,767 CEP95
    nsv5145817mobile element insertion1nstd203human GRCh38 chr17: 64,524,239-64,524,256 , GRCh37.p13 chr17|NW_003315947.1: 328,086-328,103 , GRCh37.p13 chr17: 62,520,357-62,520,374 CEP95
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv5010625copy number variation1nstd200human GRCh38 chr17: 64,536,414-64,536,512 , GRCh37.p13 chr17|NW_003315947.1: 340,261-340,359 , GRCh37.p13 chr17: 62,532,532-62,532,630 CEP95
    nsv5010624copy number variation1nstd200human GRCh38 chr17: 64,524,172-64,528,426 , GRCh37.p13 chr17|NW_003315947.1: 328,019-332,273 , GRCh37.p13 chr17: 62,520,290-62,524,544 CEP95
    nsv4619419copy number variation1nstd183human GRCh37 chr17: 62,498,030-62,502,993 , GRCh38.p12 chr17: 64,501,912-64,506,875 CEP95, DDX5
    nsv4557153insertion1nstd166human GRCh37.p13 chr17: 62,520,357-62,520,357 , GRCh38.p12 chr17: 64,524,239-64,524,239 CEP95
    nsv4532413copy number variation1nstd166human GRCh37.p13 chr17: 62,505,445-62,506,280 , GRCh38.p12 chr17: 64,509,327-64,510,162 CEP95
    nsv4512892mobile element insertion1nstd166human GRCh37.p13 chr17: 62,518,435-62,518,435 , GRCh38.p12 chr17: 64,522,317-64,522,317 CEP95
    nsv4506067mobile element insertion1nstd166human GRCh37.p13 chr17: 62,510,400-62,510,400 , GRCh38.p12 chr17: 64,514,282-64,514,282 CEP95
    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
    nsv4268220copy number variation1nstd166human GRCh37.p13 chr17: 62,517,895-62,518,277 , GRCh38.p12 chr17: 64,521,777-64,522,159 CEP95
    nsv4261157copy number variation1nstd166human GRCh37.p13 chr17: 62,494,000-62,507,000 , GRCh38.p12 chr17: 64,497,882-64,510,882 CEP95, MIR5047, 2 more genes
    nsv4260500copy number variation1nstd166human GRCh37.p13 chr17: 62,499,900-62,506,000 , GRCh38.p12 chr17: 64,503,782-64,509,882 DDX5, CEP95
    nsv4259783copy number variation1nstd166human GRCh37.p13 chr17: 62,523,855-62,524,033 , GRCh38.p12 chr17: 64,527,737-64,527,915 CEP95
    nsv4254433copy number variation1nstd166human GRCh37.p13 chr17: 62,523,919-62,523,994 , GRCh38.p12 chr17: 64,527,801-64,527,876 CEP95
    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
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