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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935781copy number variation1nstd209human GRCh38 chr14: 104,807,605-104,854,199 , GRCh37.p13 chr14: 105,273,942-105,320,536 RPS2P4, VESTAR, 1 more genes
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5274708copy number variation1nstd204human GRCh37.p13 chr14: 105,273,938-105,431,737 , GRCh38.p13 chr14: 104,807,601-104,965,400 RPS2P4, AHNAK2, 5 more genes
    nsv5005042copy number variation1nstd200human GRCh38 chr14: 104,831,519-104,840,919 , GRCh37.p13 chr14: 105,297,856-105,307,256 RPS2P4, RPS26P49
    nsv4991599copy number variation1nstd200human GRCh38 chr14: 104,834,690-104,834,792 , GRCh37.p13 chr14: 105,301,027-105,301,129 RPS2P4
    nsv4991598copy number variation1nstd200human GRCh38 chr14: 104,833,702-104,835,449 , GRCh37.p13 chr14: 105,300,039-105,301,786 RPS2P4
    nsv4991595copy number variation1nstd200human GRCh38 chr14: 104,826,143-104,835,594 , GRCh37.p13 chr14: 105,292,480-105,301,931 RPS26P49, RPS2P4
    nsv4863627copy number variation1nstd200human GRCh37 chr14: 105,297,856-105,307,256 , GRCh38.p12 chr14: 104,831,519-104,840,919 RPS2P4, RPS26P49
    nsv4855130copy number variation1nstd200human GRCh37 chr14: 105,292,480-105,301,931 , GRCh38.p12 chr14: 104,826,143-104,835,594 RPS26P49, RPS2P4
    nsv4729218copy number variation1nstd102humanPathogenic GRCh37 chr14: 102,615,953-107,285,437 , GRCh38.p12 chr14: 102,149,616-106,877,229 IGHV4-61, IGHD3-9, 308 more genes
    nsv4728966copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,204,147-105,543,486 , GRCh38.p12 chr14: 104,737,810-105,077,149 CLBA1, ZBTB42, 15 more genes
    nsv4684265copy number variation1nstd102humanPathogenic GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456 NDUFB3P4, LINC02320, 502 more genes
    nsv4681219copy number variation1nstd102humanPathogenic GRCh37 chr14: 105,143,996-105,424,009 , GRCh38.p12 chr14: 104,677,659-104,957,672 INF2, SIVA1, 14 more genes
    nsv4675524copy number variation1nstd102humanPathogenic GRCh37 chr14: 104,764,078-107,285,437 , GRCh38.p12 chr14: 104,297,741-106,877,229 IGHV3-76, IGHV5-10-1, 241 more genes
    nsv4675364copy number variation1nstd102humanPathogenic GRCh37 chr14: 105,303,584-107,285,437 , GRCh38.p12 chr14|NT_187600.1: 1-1,214,078 , GRCh38.p12 chr14: 104,837,247-106,877,229 PACS2, IGHVII-15-1, 226 more genes
    nsv4624902copy number variation1nstd183human GRCh37 chr14: 103,676,460-105,831,463 , GRCh38.p12 chr14: 103,210,123-105,365,126 , ZFYVE21, 69 more genes
    nsv4624595copy number variation1nstd183human GRCh37 chr14: 104,929,882-106,342,979 , GRCh38.p12 chr14: 104,466,471-105,877,120 , IGHJ2, 73 more genes
    nsv4456944copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,627,916-107,147,698 , GRCh38.p12 chr14: 101,161,579-106,691,681 IGHV1-58, IGHVII-60-1, 308 more genes
    nsv4456320copy number variation1nstd102humanPathogenic GRCh37 chr14: 102,931,119-107,285,437 , GRCh38.p12 chr14: 102,464,782-106,877,229 LOC105378184, LINC02298, 302 more genes
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
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