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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6530598copy number variation1nstd223human GRCh38 chr17: 56,592,301-56,593,700 , GRCh37.p13 chr17: 54,669,662-54,671,061 NOG
    nsv6310393copy number variation1nstd102humanUncertain significance GRCh37 chr17: 54,671,585-59,938,900 , GRCh38.p12 chr17: 56,594,224-61,861,539 RNF43, LOC107985048, 132 more genes
    nsv6133360copy number variation1nstd213human GRCh37 chr17: 54,490,000-54,740,001 , GRCh38.p12 chr17: 56,412,639-56,662,640 NOG, ANKFN1, 2 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 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
    nsv4769284copy number variation1nstd102humanPathogenic GRCh37 chr17: 54,290,100-54,844,894 , GRCh38.p12 chr17: 56,212,739-56,767,533 ANKFN1, NOG, 2 more genes
    nsv4729900copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 54,664,412-54,705,223 , GRCh38.p12 chr17: 56,587,051-56,627,862 NOG
    nsv4673596copy number variation1nstd186human GRCh37 chr17: 54,670,101-54,675,500 , GRCh38.p12 chr17: 56,592,740-56,598,139 NOG
    nsv4634219copy number variation1nstd183human GRCh37 chr17: 54,670,101-54,675,500 , GRCh38.p12 chr17: 56,592,740-56,598,139 NOG
    nsv4421948copy number variation1nstd174human GRCh37 chr17: 54,669,945-54,675,692 , GRCh38.p12 chr17: 56,592,584-56,598,331 NOG
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv3920880copy number variation1nstd102humanPathogenic GRCh38 chr17: 49,974,533-56,807,609 , NCBI36 chr17: 45,406,896-52,239,969 , GRCh37 chr17: 48,051,897-54,884,970 LOC107984983, LOC102724732, 85 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
    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
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 FOXK2, SOCS3-DT, 958 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
    nsv3904574copy number variation1nstd102humanPathogenic GRCh37 chr17: 54,584,318-55,220,914 , GRCh38.p12 chr17: 56,506,957-57,143,553 RNF126P1, LOC105371836, 14 more genes
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