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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6997956copy number variation1nstd229human GRCh38 chr17: 35,872,662-35,880,963 , GRCh37.p13 chr17|NW_004166864.2: 164,830-173,131 CCL5
    nsv6990791copy number variation1nstd229human GRCh38 chr17: 35,872,464-35,878,527 , GRCh37.p13 chr17|NW_004166864.2: 164,632-170,695 CCL5
    nsv6624075copy number variation1nstd224human GRCh37 chr17: 34,195,180-34,207,486 , GRCh38.p12 chr17: 35,868,176-35,880,482 , GRCh38.p12 chr17|NT_187614.1: 102,708-115,014 CCL5, HEATR9
    nsv6510305copy number variation1nstd223human GRCh38 chr17: 35,822,938-36,193,984 , GRCh37.p13 chr17: 34,246,253-34,442,620 , LOC107985068, 26 more genes
    nsv6509123copy number variation1nstd223human GRCh38 chr17: 35,869,283-35,873,232 , GRCh37.p13 chr17|NW_004166864.2: 161,451-165,400 CCL5, HEATR9
    nsv6133353copy number variation1nstd213human GRCh37 chr17: 33,210,000-34,670,001 , GRCh38.p12 chr17: 34,882,981-35,919,248 AP2B1, E2F3P1, 48 more genes
    nsv6133052copy number variation1nstd213human GRCh37 chr17: 33,850,000-34,430,001 , GRCh38.p12 chr17: 35,522,981-35,919,248 RASL10B, RDM1, 21 more genes
    nsv6133050copy number variation1nstd213human GRCh37 chr17: 32,790,000-34,510,001 , GRCh38.p12 chr17: 34,462,981-35,919,248 AP2B1, E2F3P1, 53 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5522788copy number variation1nstd206human GRCh38 chr17: 35,879,037-35,882,406 , GRCh37.p13 chr17|NW_004166864.2: 171,205-174,574 , CCL5
    nsv5016153copy number variation1nstd200human GRCh38 chr17: 35,869,283-35,873,214 , GRCh37.p13 chr17|NW_004166864.2: 161,451-165,382 , CCL5, 1 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 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
    nsv4244076copy number variation1nstd166human GRCh37.p13 chr17: 34,058,749-34,328,565 , GRCh38.p12 chr17: 35,731,730-35,919,248 , GRCh38.p12 chr17|NT_187614.1: 1-153,780 , CCL5, 13 more genes
    nsv3919991copy number variation1nstd102humanUncertain significance NCBI36 chr17: 31,198,036-31,323,231 , GRCh37.p13 chr17|NW_004166864.2: 139,087-211,416 , GRCh37.p13 chr17: 34,173,923-34,299,118 , GRCh38.p12 chr17: 35,846,919-35,919,248 , GRCh38.p12 chr17|NT_187614.1: 81,451-153,780 HEATR9, LRRC37A9P, 7 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
    nsv3907376copy number variation1nstd102humanUncertain significance GRCh37 chr17: 32,351,496-34,455,576 , GRCh38.p12 chr17: 34,024,477-35,919,248 CCL8, TAF5LP1, 67 more genes
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