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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142489insertion1nstd232human GRCh37.p13 chr17: 49,371,408-49,371,408 , GRCh38.p12 chr17: 51,294,047-51,294,047 UTP18
    nsv6992977copy number variation1nstd229human GRCh38 chr17: 51,275,750-51,276,355 , GRCh37.p13 chr17: 49,353,111-49,353,716 UTP18
    nsv6992766copy number variation1nstd229human GRCh38 chr17: 51,278,576-51,279,914 , GRCh37.p13 chr17: 49,355,937-49,357,275 UTP18
    nsv6986384copy number variation1nstd229human GRCh38 chr17: 49,089,556-55,863,152 , GRCh37.p13 chr17: 47,166,918-53,940,513 LOC107985002, FAM117A, 107 more genes
    nsv6981559copy number variation1nstd229human GRCh38 chr17: 51,292,850-51,678,463 , GRCh37.p13 chr17: 49,370,211-49,755,823 LINC02072, RPL7P48, 4 more genes
    nsv6587032inversion1nstd223human GRCh38 chr17: 51,274,476-51,275,073 , GRCh37.p13 chr17: 49,351,837-49,352,434 UTP18
    nsv6527906copy number variation1nstd223human GRCh38 chr17: 51,264,835-51,265,737 , GRCh37.p13 chr17: 49,342,196-49,343,098 UTP18
    nsv6523651copy number variation1nstd223human GRCh38 chr17: 51,290,275-51,291,509 , GRCh37.p13 chr17: 49,367,636-49,368,870 UTP18
    nsv6519005copy number variation1nstd223human GRCh38 chr17: 51,292,850-51,678,463 , GRCh37.p13 chr17: 49,370,211-49,755,823 RPL7P48, LINC02073, 4 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
    nsv5026419copy number variation1nstd200human GRCh38 chr17: 51,289,088-51,290,951 , GRCh37.p13 chr17: 49,366,449-49,368,312 UTP18
    nsv5026418copy number variation1nstd200human GRCh38 chr17: 51,262,216-51,262,274 , GRCh37.p13 chr17: 49,339,577-49,339,635 UTP18
    nsv5013815copy number variation1nstd200human GRCh38 chr17: 51,283,406-51,284,030 , GRCh37.p13 chr17: 49,360,767-49,361,391 UTP18
    nsv4867282copy number variation1nstd200human GRCh37 chr17: 49,366,602-49,366,859 , GRCh38.p12 chr17: 51,289,241-51,289,498 UTP18
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4257928copy number variation1nstd166human GRCh37.p13 chr17: 49,339,577-49,339,635 , GRCh38.p12 chr17: 51,262,216-51,262,274 UTP18
    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
    nsv3912763copy number variation1nstd102humanPathogenic NCBI36 chr17: 44,570,225-47,580,169 , GRCh37 chr17: 47,215,226-50,225,170 , GRCh38 chr17: 49,137,864-52,147,810 CACNA1G, SUMO2P7, 77 more genes
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