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Items: 1 to 20 of 97

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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
    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
    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
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 P4HB, LOC105371808, 2366 more genes
    nsv3899598copy number variation1nstd102humanBenign GRCh37 chr17: 34,205,640-34,245,061 , GRCh38.p12 chr17: 35,878,636-35,918,057 , GRCh38.p12 chr17|NT_187614.1: 113,168-152,589 RDM1, LRRC37A8P, 4 more genes
    nsv3147730copy number variation1nstd151human GRCh37 chr17: 34,189,953-34,205,648 , GRCh38.p12 chr17: 35,862,949-35,878,644 , GRCh38.p12 chr17|NT_187614.1: 97,481-113,176 , CCL5, 1 more genes
    esv4010318copy number variation1estd233human GRCh37 chr17: 34,035,000-34,457,000 , GRCh38.p12 chr17: 35,707,981-35,919,248 , AP2B1, 15 more genes
    esv3879509copy number variation1estd219human GRCh37 chr17: 34,194,262-34,200,327 , GRCh38.p12 chr17: 35,867,258-35,873,323 , GRCh38.p12 chr17|NT_187614.1: 101,790-107,855 , CCL5, 1 more genes
    nsv1869604short tandem repeat2nstd128human GRCh37 chr17: 34,202,043-34,202,053 , GRCh38.p12 chr17|NT_187614.1: 109,571-109,581 , GRCh38.p12 chr17: 35,875,039-35,875,049 , CCL5
    nsv1869603short tandem repeat4nstd128human GRCh37 chr17: 34,197,641-34,197,655 , GRCh38.p12 chr17: 35,870,637-35,870,651 , GRCh38.p12 chr17|NT_187614.1: 105,169-105,183 , CCL5
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