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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5872401copy number variation1nstd209human GRCh38 chr17: 40,963,692-40,970,508 , GRCh37.p13 chr17: 39,119,944-39,126,760 LOC107985072, KRT39
    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
    nsv5515865copy number variation1nstd206human GRCh38 chr17: 40,961,102-40,961,208 , GRCh37.p13 chr17: 39,117,354-39,117,460 KRT39, LOC107985072
    nsv5154551mobile element insertion1nstd203human GRCh38 chr17: 40,965,464-40,965,481 , GRCh37.p13 chr17: 39,121,716-39,121,733 LOC107985072, KRT39
    nsv5016351copy number variation1nstd200human GRCh38 chr17: 40,961,102-40,961,208 , GRCh37.p13 chr17: 39,117,354-39,117,460 LOC107985072, KRT39
    nsv5016348copy number variation1nstd200human GRCh38 chr17: 40,915,880-40,961,156 , GRCh37.p13 chr17: 39,072,132-39,117,408 LOC107985072, KRT39, 2 more genes
    nsv5016346copy number variation1nstd200human GRCh38 chr17: 40,909,717-40,979,608 , GRCh37.p13 chr17: 39,065,969-39,135,860 LOC105371777, LOC107985072, 3 more genes
    nsv4858800copy number variation1nstd200human GRCh37 chr17: 39,065,969-39,135,860 , GRCh38.p12 chr17|NW_003871091.1: 58,985-129,003 , GRCh38.p12 chr17: 40,909,717-40,979,608 KRT23, KRT39, 3 more genes
    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
    nsv4624934copy number variation1nstd183human GRCh37 chr17: 39,066,040-39,132,240 , GRCh38.p12 chr17: 40,909,788-40,975,988 , GRCh38.p12 chr17|NW_003871091.1: 59,056-125,383 LOC107985072, KRT23, 3 more genes
    nsv4369012copy number variation1nstd173human GRCh37 chr17: 39,071,587-39,116,603 , GRCh38.p12 chr17: 40,915,335-40,960,351 , GRCh38.p12 chr17|NW_003871091.1: 64,603-109,746 KRT23, LOC107985072, 2 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
    nsv4265480copy number variation1nstd166human GRCh37.p13 chr17: 39,117,354-39,117,460 , GRCh38.p12 chr17|NW_003871091.1: 110,497-110,603 , GRCh38.p12 chr17: 40,961,102-40,961,208 LOC107985072, KRT39
    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
    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
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