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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3115935copy number variation1nstd145human GRCh37 chr3: 85,141,719-85,385,120 , GRCh38.p12 chr3: 85,092,568-85,335,970 CADM2
    nsv3110870copy number variation1nstd145human GRCh37 chrX: 22,602,740-22,694,618 , GRCh38.p12 chrX: 22,584,623-22,676,501 PTCHD1-AS
    nsv3110971copy number variation6nstd145human GRCh37 chr11: 97,820,128-97,876,272 , GRCh38.p12 chr11: 97,949,128-98,005,544 LINC02713
    nsv3115889copy number variation6nstd145human GRCh37 chr20: 1,561,593-1,593,968 , GRCh38.p12 chr20: 1,580,947-1,613,322 SIRPB1
    nsv3110530copy number variation2nstd145human GRCh37 chr16: 55,797,365-55,813,048 , GRCh38.p12 chr16: 55,763,453-55,779,136 CES1P1
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3117380copy number variation44nstd145human GRCh37 chr21: 23,655,218-23,665,891 , GRCh38.p12 chr21: 22,282,898-22,293,571 , GRCh38.p12 chr21|NW_003315968.2: 187,127-197,800 LOC107985508
    nsv3118025copy number variation35nstd145human GRCh37 chr8: 15,402,271-15,412,465 , GRCh38.p12 chr8: 15,544,762-15,554,956 TUSC3
    nsv3113893copy number variation2nstd145human GRCh37 chr9: 20,794,561-20,804,551 , GRCh38.p12 chr9: 20,794,562-20,804,552 FOCAD
    nsv3113430copy number variation1nstd145human GRCh37 chr1: 231,535,936-231,545,858 , GRCh38.p12 chr1: 231,400,190-231,410,112 EGLN1
    nsv3112394copy number variation1nstd145human GRCh37 chr1: 196,738,156-196,745,701 , GRCh38.p12 chr1: 196,769,026-196,776,571 CFHR3
    nsv3114475copy number variation50nstd145human GRCh37 chr5: 12,811,448-12,818,768 , GRCh38.p12 chr5: 12,811,336-12,818,656 LOC105374657
    nsv3115274copy number variation1nstd145human GRCh37 chr7: 110,181,699-110,188,346 , GRCh38.p12 chr7: 110,541,642-110,548,289 LOC105375451
    nsv3112146copy number variation37nstd145human GRCh37 chr11: 93,695,236-93,701,577 , GRCh38.p12 chr11: 93,962,070-93,968,411 LOC101060084
    nsv3116610copy number variation4nstd145human GRCh37 chr7: 112,592-118,247 , GRCh38.p12 chr7|NT_187558.1: 68,352-74,169 , GRCh38.p12 chr7|NT_187653.1: 104,913-110,568 , GRCh38.p12 chr7: 112,592-118,247 LOC105375114
    nsv3112488copy number variation14nstd145human GRCh37 chr7: 16,794,950-16,800,421 , GRCh38.p12 chr7: 16,755,325-16,760,796 TSPAN13
    nsv3110401copy number variation14nstd145human GRCh37 chr5: 11,129,609-11,134,869 , GRCh38.p12 chr5: 11,129,497-11,134,757 CTNND2
    nsv3118312copy number variation2nstd145human GRCh37 chr2: 49,534,108-49,539,079 , GRCh38.p12 chr2: 49,306,969-49,311,940 LOC105374595
    nsv3116148copy number variation97nstd145human GRCh37 chr8: 594,429-599,002 , GRCh38.p12 chr8: 644,429-649,002 ERICH1
    nsv3115553copy number variation167nstd145human GRCh37 chr22: 37,143,594-37,146,950 , GRCh38.p12 chr22: 36,747,550-36,750,906 CACNG2-DT
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