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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5886497copy number variation1nstd209human GRCh38 chr17: 40,436,238-40,448,095 , GRCh37.p13 chr17: 38,592,490-38,604,347 IGFBP4, RPL23AP75
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv4623206copy number variation1nstd183human GRCh37 chr17: 38,588,234-38,671,817 , GRCh38.p12 chr17: 40,431,982-40,515,565 , TNS4, 3 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
    nsv4269521copy number variation1nstd166human GRCh37.p13 chr17: 38,592,505-38,605,948 , GRCh38.p12 chr17: 40,436,253-40,449,696 RPL23AP75, IGFBP4
    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
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
    nsv3911344copy number variation1nstd102humanPathogenic GRCh37 chr17: 37,356,126-43,706,945 , NCBI36 chr17: 34,609,652-41,062,728 , GRCh38 chr17: 39,199,873-45,629,579 IFI35, RND2, 345 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
    nsv3903749copy number variation1nstd102humanLikely benign GRCh37 chr17: 38,543,535-38,785,943 , GRCh38.p12 chr17: 40,387,283-40,629,691 IGFBP4, TOP2A, 6 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
    nsv3165835copy number variation1nstd151human GRCh37 chr17: 38,348,462-39,021,219 , GRCh38.p12 chr17: 40,192,210-40,864,967 , CDC6, 33 more genes
    nsv3164017copy number variation1nstd151human GRCh37 chr17: 38,609,234-38,652,682 , GRCh38.p12 chr17: 40,452,982-40,496,430 , IGFBP4, 1 more genes
    nsv3162485copy number variation1nstd151human GRCh37 chr17: 37,093,425-39,018,015 , GRCh38.p12 chr17: 38,937,172-40,861,763 , CCR7, 83 more genes
    nsv3158597copy number variation1nstd151human GRCh37 chr17: 38,609,234-38,933,989 , GRCh38.p12 chr17: 40,452,982-40,777,737 , KRT222, 13 more genes
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