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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5717090mobile element insertion1nstd211human GRCh38 chr16: 28,730,609-28,730,609 , GRCh37.p13 chr16: 28,741,930-28,741,930 EIF3C
    nsv5673078copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,488,827-28,950,294 , GRCh38.p12 chr16: 28,477,506-28,938,973 SH2B1, NUPR1, 21 more genes
    nsv5672755copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 28,668,059-29,001,338 , GRCh38.p12 chr16: 28,656,738-28,990,017 ATP2A1, CD19, 17 more genes
    nsv5597999copy number variation1nstd207human GRCh38 chr16: 28,698,452-28,709,337 , GRCh37.p13 chr16: 28,709,773-28,720,658 CDC37P1, EIF3C
    nsv5597413copy number variation1nstd207human GRCh38 chr16: 28,698,281-28,698,595 , GRCh37.p13 chr16: 28,709,602-28,709,916 EIF3C
    nsv5589785copy number variation1nstd207human GRCh38 chr16: 28,735,019-28,735,069 , GRCh37.p13 chr16: 28,746,340-28,746,390 EIF3C, NPIPB9
    nsv5524193copy number variation1nstd206human GRCh38 chr16: 28,731,986-28,756,986 , GRCh37.p13 chr16: 28,743,307-28,768,307 , EIF3C, 2 more genes
    nsv5329771translocation1nstd200human GRCh37 chr3: 5,033,886-5,033,886 , GRCh37 chr16: 28,710,821-28,710,821 , GRCh38.p12 chr16: 28,699,500-28,699,500 , GRCh38.p12 chr3: 4,992,201-4,992,201 , EIF3C, 1 more genes
    nsv5279789copy number variation1nstd204human GRCh38.p13 chr16: 28,699,401-28,701,300 , GRCh37.p13 chr16: 28,710,722-28,712,621 CDC37P1, EIF3C
    nsv5279548copy number variation1nstd204human GRCh38.p13 chr16: 28,733,001-28,737,900 , GRCh37.p13 chr16: 28,744,322-28,749,221 EIF3C, NPIPB9
    nsv5279532copy number variation1nstd204human GRCh38.p13 chr16: 28,709,601-28,752,500 , GRCh37.p13 chr16: 28,720,922-28,763,821 , MIR6862-2, 3 more genes
    nsv5279332copy number variation1nstd204human GRCh38.p13 chr16: 28,701,101-28,704,300 , GRCh37.p13 chr16: 28,712,422-28,715,621 EIF3C, CDC37P1
    nsv5278437copy number variation1nstd204human GRCh38.p13 chr16: 28,695,201-28,697,300 , GRCh37.p13 chr16: 28,706,522-28,708,621 EIF3C
    nsv5278347copy number variation1nstd204human GRCh38.p13 chr16: 28,698,301-28,698,800 , GRCh37.p13 chr16: 28,709,622-28,710,121 EIF3C
    nsv5278030copy number variation1nstd204human GRCh38.p13 chr16: 28,695,401-28,704,800 , GRCh37.p13 chr16: 28,706,722-28,716,121 CDC37P1, EIF3C
    nsv5277754copy number variation1nstd204human GRCh38.p13 chr16: 28,690,501-28,701,800 , GRCh37.p13 chr16: 28,701,822-28,713,121 CDC37P1, EIF3C
    nsv5276900copy number variation1nstd204human GRCh38.p13 chr16: 28,697,201-28,703,900 , GRCh37.p13 chr16: 28,708,522-28,715,221 CDC37P1, EIF3C
    nsv5276825copy number variation1nstd204human GRCh38.p13 chr16: 28,685,001-28,691,600 , GRCh37.p13 chr16: 28,696,322-28,702,921 EIF3C
    nsv5276337copy number variation1nstd204human GRCh38.p13 chr16: 28,727,301-28,731,500 , GRCh37.p13 chr16: 28,738,622-28,742,821 EIF3C
    nsv5275996copy number variation1nstd204human GRCh38.p13 chr16: 28,697,501-28,699,800 , GRCh37.p13 chr16: 28,708,822-28,711,121 EIF3C, CDC37P1
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