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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5297565copy number variation1nstd204human GRCh38.p13 chr17: 5,436,401-5,488,300 , GRCh37.p13 chr17: 5,339,721-5,391,620 DHX33, MIS12, 3 more genes
    nsv5031337inversion1nstd200human GRCh38 chr17: 5,462,212-6,246,469 , GRCh37.p13 chr17: 5,365,532-6,149,789 NLRP1, DHX33-DT, 12 more genes
    nsv5015651copy number variation1nstd200human GRCh38 chr17: 5,476,155-5,477,552 , GRCh37.p13 chr17: 5,379,475-5,380,872 DERL2
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729877copy number variation1nstd102humanUncertain significance GRCh37 chr17: 5,143,295-5,850,209 , GRCh38.p12 chr17: 5,240,000-5,946,889 DHX33, MIS12, 14 more genes
    nsv4675776copy number variation1nstd102humanUncertain significance GRCh37 chr17: 5,378,522-5,692,834 , GRCh38.p12 chr17: 5,475,202-5,789,514 RNU7-31P, MIS12, 7 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 SRR, DBIL5P, 196 more genes
    nsv4630208copy number variation1nstd183human GRCh37 chr17: 4,486,568-5,620,052 , GRCh38.p12 chr17: 4,583,273-5,716,732 , ARRB2, 59 more genes
    nsv4457587copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,759,126-6,128,911 , GRCh38.p12 chr17: 3,855,832-6,225,591 DERL2, ZZEF1, 82 more genes
    nsv4375536copy number variation1nstd173human GRCh37 chr17: 5,381,867-5,427,846 , GRCh38.p12 chr17: 5,478,547-5,524,526 LOC728392, LOC101928044, 4 more genes
    nsv4350781copy number variation1nstd102humanPathogenic GRCh37 chr17: 47,546-6,287,620 , GRCh38.p12 chr17: 197,755-6,384,300 SERPINF1, UBE2G1, 201 more genes
    nsv4240234copy number variation1nstd166human GRCh37.p13 chr17: 5,387,000-5,392,000 , GRCh38.p12 chr17: 5,483,680-5,488,680 DERL2, MIS12
    nsv4237568copy number variation1nstd166human GRCh37.p13 chr17: 5,379,475-5,380,872 , GRCh38.p12 chr17: 5,476,155-5,477,552 DERL2
    nsv4236002copy number variation1nstd166human GRCh37.p13 chr17: 5,389,675-5,389,799 , GRCh38.p12 chr17: 5,486,355-5,486,479 DERL2, MIS12
    nsv3923152copy number variation1nstd102humanPathogenic NCBI36 chr17: 3,451,558-7,022,067 , GRCh38 chr17: 3,601,515-7,178,024 , GRCh37 chr17: 3,504,809-7,081,343 PSMB6, NUP88, 133 more genes
    nsv3922546copy number variation1nstd102humanPathogenic NCBI36 chr17: 525-5,779,421 , GRCh38 chr17: 150,732-5,935,377 , GRCh37 chr17: 525-5,838,697 CHRNE, SPNS2-AS1, 198 more genes
    nsv3917777copy number variation1nstd102humanPathogenic GRCh37 chr17: 50,690-7,394,448 , GRCh38 chr17: 198,748-7,491,129 , NCBI36 chr17: 48,539-7,335,172 PAFAH1B1, PELP1-DT, 267 more genes
    nsv3917059copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901 PSMB6, RNU6-1065P, 409 more genes
    nsv3916209copy number variation1nstd102humanLikely pathogenic NCBI36 chr17: 3,894,345-5,787,816 , GRCh37 chr17: 3,947,596-5,847,092 , GRCh38 chr17: 4,044,302-5,943,772 ALOX15, ARRB2, 75 more genes
    nsv3915884copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-6,862,369 , GRCh38 chr17: 162,088-6,959,050 , NCBI36 chr17: 11,879-6,803,093 LOC105371592, CAMKK1, 222 more genes
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