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    Number of Variants: 10

    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 CCL5, PSMD11, 117 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 CCL5, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 CCL5, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 CCL5, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 CCL5, SMURF2, 2366 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 CCL5, LOC105371922, 1855 more genes
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 CCL5, LOC105371753, 474 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 CCL5, RDM1, 4 more genes
    nsv3907376copy number variation1nstd102humanUncertain significance GRCh37 chr17: 32,351,496-34,455,576 , GRCh38.p12 chr17: 34,024,477-35,919,248 CCL5, CCL8, 67 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 CCL5, HEATR9, 7 more genes
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