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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv7066656inversion1nstd229human GRCh38 chr17: 40,822,205-41,582,529 , GRCh37.p13 chr17: 38,978,457-39,738,781 LOC105371777, KRT10, 69 more genes
    nsv6995385copy number variation1nstd229human GRCh38 chr17: 41,003,912-41,025,589 , GRCh37.p13 chr17: 39,160,164-39,181,841 KRTAP3-1, KRTAP3-4P, 1 more genes
    nsv6992218copy number variation1nstd229human GRCh38 chr17: 40,934,745-41,023,836 , GRCh37.p13 chr17: 39,090,997-39,180,088 KRT40, KRTAP3-1, 6 more genes
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6980978copy number variation1nstd229human GRCh38 chr17: 41,008,529-41,008,718 , GRCh37.p13 chr17: 39,164,781-39,164,970 KRTAP3-1
    nsv6980804copy number variation1nstd229human GRCh38 chr17: 40,949,294-41,074,654 , GRCh37.p13 chr17: 39,105,546-39,230,906 KRTAP3-3, KRTAP3-1, 14 more genes
    nsv6509451copy number variation1nstd223human GRCh38 chr17: 40,934,745-41,023,836 , GRCh37.p13 chr17: 39,090,997-39,180,088 KRT23, KRTAP3-2, 6 more genes
    nsv6133056copy number variation1nstd213human GRCh37 chr17: 36,400,000-39,740,001 , GRCh38.p12 chr17: 38,545,381-41,583,749 CACNB1, CDC6, 176 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
    nsv5518631copy number variation1nstd206human GRCh38 chr17: 40,902,081-41,114,453 , GRCh37.p13 chr17: 39,058,333-39,270,705 KRTAP2-3, LOC105371777, 20 more genes
    nsv5192615mobile element insertion1nstd203human GRCh38 chr17: 41,008,004-41,008,021 , GRCh37.p13 chr17: 39,164,256-39,164,273 KRTAP3-1
    nsv5013696copy number variation1nstd200human GRCh38 chr17: 41,002,412-41,010,880 , GRCh37.p13 chr17: 39,158,664-39,167,132 KRTAP3-4P, KRTAP3-1
    nsv4679355copy number variation1nstd189human GRCh37.p13 chr17: 38,659,900-39,414,647 , GRCh38.p12 chr17: 40,503,648-41,258,395 , CCR7, 54 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
    nsv3918835copy number variation1nstd102humanLikely benign GRCh38 chr17: 40,927,571-41,313,858 , NCBI36 chr17: 36,337,349-36,723,636 , GRCh37 chr17: 39,083,823-39,470,110 KRTAP9-2, KRTAP3-3, 42 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
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