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Items: 1 to 20 of 127

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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
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675787copy number variation1nstd102humanUncertain significance GRCh37 chr17: 34,158,619-34,477,480 , GRCh38.p12 chr17: 35,919,249-36,150,098 , GRCh38.p12 chr17|NT_187614.1: 153,781-385,008 CCL4, CCL3-AS1, 15 more genes
    nsv4634127copy number variation1nstd183human GRCh37 chr17: 34,151,274-34,485,091 , GRCh38.p12 chr17: 35,919,249-36,157,718 , GRCh38.p12 chr17|NT_187614.1: 153,781-392,619 , RDM1, 16 more genes
    nsv4631441copy number variation1nstd183human GRCh37 chr17: 34,149,960-34,475,514 , GRCh38.p12 chr17: 35,919,249-36,148,133 , GRCh38.p12 chr17|NT_187614.1: 153,781-383,042 , CCL14, 16 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
    nsv4457542copy number variation1nstd102humanUncertain significance GRCh37 chr17: 34,151,183-34,477,480 , GRCh38.p12 chr17: 35,919,249-36,150,098 , GRCh38.p12 chr17|NT_187614.1: 153,781-385,008 CCL14, LOC101927369, 15 more genes
    nsv4380150copy number variation1nstd173human GRCh37 chr17: 34,151,081-34,477,480 , GRCh38.p12 chr17: 35,919,249-36,150,098 , GRCh38.p12 chr17|NT_187614.1: 153,781-385,008 , CCL4, 16 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
    nsv3968589insertion1nstd168human GRCh38 chr17: 35,964,643-35,989,019 , GRCh37.p13 chr17: 34,291,661-34,316,055 CCL14, CCL16, 1 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
    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
    nsv3211998copy number variation1nstd152human GRCh38 chr17: 35,973,275-35,989,019 , GRCh37.p13 chr17: 34,300,305-34,316,055 CCL14, CCL16, 1 more genes
    nsv3153966copy number variation1nstd151human GRCh37 chr17: 34,304,599-34,433,668 , GRCh38.p12 chr17: 35,977,563-36,106,275 , GRCh38.p12 chr17|NT_187614.1: 212,127-341,196 CCL14, CCL23, 10 more genes
    nsv3148927copy number variation1nstd151human GRCh37 chr17: 34,173,907-34,433,668 , GRCh38.p12 chr17: 35,919,249-36,106,275 , GRCh38.p12 chr17|NT_187614.1: 153,781-341,196 CCL23, CCL3-AS1, 12 more genes
    nsv3143873copy number variation1nstd151human GRCh37 chr17: 34,304,599-34,305,304 , GRCh38.p12 chr17|NT_187614.1: 212,127-212,832 , GRCh38.p12 chr17: 35,977,563-35,978,268 CCL16
    nsv3139357copy number variation1nstd151human GRCh37 chr17: 34,304,599-34,398,406 , GRCh38.p12 chr17: 35,977,563-36,071,046 , GRCh38.p12 chr17|NT_187614.1: 212,127-305,934 LOC107985068, CCL16, 6 more genes
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