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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945175copy number variation1nstd209human GRCh38 chr14: 105,477,854-105,477,907 , GRCh37.p13 chr14|NW_004166863.1: 141,021-141,074 , GRCh37.p13 chr14: 105,944,191-105,944,244 CRIP2
    nsv5654338insertion2nstd207human GRCh38 chr14: 105,477,719-105,477,719 , GRCh37.p13 chr14|NW_004166863.1: 140,886-140,886 , GRCh37.p13 chr14: 105,944,056-105,944,056 CRIP2
    nsv5645180insertion1nstd207human GRCh38 chr14: 105,477,700-105,477,700 , GRCh37.p13 chr14|NW_004166863.1: 140,867-140,867 , GRCh37.p13 chr14: 105,944,037-105,944,037 CRIP2
    nsv5601771copy number variation1nstd207human GRCh38 chr14: 105,477,854-105,477,907 , GRCh37.p13 chr14|NW_004166863.1: 141,021-141,074 , GRCh37.p13 chr14: 105,944,191-105,944,244 CRIP2
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv4991656copy number variation1nstd200human GRCh38 chr14: 105,479,684-105,479,854 , GRCh37.p13 chr14|NW_004166863.1: 142,851-143,021 , GRCh37.p13 chr14: 105,946,021-105,946,191 CRIP2
    nsv4991641copy number variation1nstd200human GRCh38 chr14: 105,300,301-106,578,744 , GRCh37.p13 chr14: 105,766,638-106,929,356 , GRCh37.p13 chr14|NW_004166863.1: 1-1,025,122 , IGHV1-18, 165 more genes
    nsv4764542insertion1nstd199human GRCh37 chr14: 105,944,010-105,944,010 , GRCh38.p12 chr14: 105,477,673-105,477,673 CRIP2
    nsv4747712copy number variation1nstd199human GRCh37 chr14: 105,944,010-105,944,835 , GRCh38.p12 chr14: 105,477,673-105,478,498 CRIP2
    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
    nsv4728126copy number variation1nstd197human GRCh38.p12 chr14: 105,478,980-105,479,653 , GRCh37 chr14: 105,945,317-105,945,990 CRIP2
    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
    nsv4675811copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,690,721-106,019,451 , GRCh38.p12 chr14: 105,224,384-105,533,002 TEDC1, MTA1, 10 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
    nsv4651945copy number variation1nstd186human GRCh37 chr14: 105,940,019-105,950,877 , GRCh38.p12 chr14: 105,473,682-105,484,540 CRIP2
    nsv4630298copy number variation1nstd183human GRCh37 chr14: 105,843,057-105,941,002 , GRCh38.p12 chr14: 105,376,720-105,474,665 MTA1, PACS2, 3 more genes
    nsv4627941copy number variation1nstd183human GRCh37 chr14: 105,848,891-106,199,376 , GRCh38.p12 chr14|NT_187600.1: 1-200,808 , GRCh38.p12 chr14: 105,382,554-105,605,042 , CRIP2, 26 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
    nsv4623384copy number variation1nstd183human GRCh37 chr14: 105,944,638-105,945,150 , GRCh38.p12 chr14: 105,478,301-105,478,813 CRIP2
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