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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5937094copy number variation1nstd209human GRCh38 chr16: 57,568,322-57,568,378 , GRCh37.p13 chr16: 57,602,234-57,602,290 LOC105371291, ADGRG5
    nsv5936574copy number variation1nstd209human GRCh38 chr16: 57,569,807-57,570,007 , GRCh37.p13 chr16: 57,603,719-57,603,919 LOC105371291, ADGRG5
    nsv5650898insertion1nstd207human GRCh38 chr16: 57,569,523-57,569,523 , GRCh37.p13 chr16: 57,603,435-57,603,435 LOC105371291, ADGRG5
    nsv5530293copy number variation1nstd206human GRCh38 chr16: 57,535,703-57,535,780 , GRCh37.p13 chr16: 57,569,615-57,569,692 CCDC102A, ADGRG5
    nsv5527022copy number variation1nstd206human GRCh38 chr16: 57,569,542-57,569,888 , GRCh37.p13 chr16: 57,603,454-57,603,800 LOC105371291, ADGRG5
    nsv5517648copy number variation1nstd206human GRCh38 chr16: 57,568,438-57,569,480 , GRCh37.p13 chr16: 57,602,350-57,603,392 ADGRG5, LOC105371291
    nsv5516606copy number variation1nstd206human GRCh38 chr16: 57,568,541-57,569,198 , GRCh37.p13 chr16: 57,602,453-57,603,110 LOC105371291, ADGRG5
    nsv5515109copy number variation1nstd206human GRCh38 chr16: 57,569,072-57,569,478 , GRCh37.p13 chr16: 57,602,984-57,603,390 ADGRG5, LOC105371291
    nsv5305720copy number variation1nstd204human GRCh37.p13 chr16: 57,463,321-57,588,854 , GRCh38.p13 chr16: 57,429,409-57,554,942 POLR2C, DOK4, 4 more genes
    nsv5277685copy number variation1nstd204human GRCh38.p13 chr16: 57,516,929-57,553,397 , GRCh37.p13 chr16: 57,550,841-57,587,309 ADGRG5, CCDC102A
    nsv5264319copy number variation1nstd204human GRCh38.p13 chr16: 57,566,901-57,569,200 , GRCh37.p13 chr16: 57,600,813-57,603,112 ADGRG5, LOC105371291
    nsv5008402copy number variation1nstd200human GRCh38 chr16: 57,571,435-57,574,754 , GRCh37.p13 chr16: 57,605,347-57,608,666 LOC105371291, ADGRG5
    nsv5008401copy number variation1nstd200human GRCh38 chr16: 57,568,772-57,569,996 , GRCh37.p13 chr16: 57,602,684-57,603,908 ADGRG5, LOC105371291
    nsv5008400copy number variation1nstd200human GRCh38 chr16: 57,560,834-57,560,979 , GRCh37.p13 chr16: 57,594,746-57,594,891 ADGRG5
    nsv5008399copy number variation1nstd200human GRCh38 chr16: 57,545,118-57,560,048 , GRCh37.p13 chr16: 57,579,030-57,593,960 ADGRG5
    nsv5005703copy number variation1nstd200human GRCh38 chr16: 57,429,638-57,554,725 , GRCh37.p13 chr16: 57,463,550-57,588,637 DOK4, COQ9, 4 more genes
    nsv4864170copy number variation1nstd200human GRCh37 chr16: 57,463,550-57,588,637 , GRCh38.p12 chr16: 57,429,638-57,554,725 DOK4, POLR2C, 4 more genes
    nsv4857216copy number variation1nstd200human GRCh37 chr16: 57,602,600-57,603,881 , GRCh38.p12 chr16: 57,568,688-57,569,969 LOC105371291, ADGRG5
    nsv4857215copy number variation1nstd200human GRCh37 chr16: 57,602,802-57,603,532 , GRCh38.p12 chr16: 57,568,890-57,569,620 ADGRG5, LOC105371291
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