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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3110568copy number variation2nstd145human GRCh37 chr1: 72,601,491-72,647,020 , GRCh38.p12 chr1: 72,135,808-72,181,337 NEGR1
    nsv3112221copy number variation11nstd145human GRCh37 chr1: 72,798,207-72,811,712 , GRCh38.p12 chr1: 72,332,524-72,346,029 , GRCh38.p12 chr1|NW_018654707.1: 44,791-67,254 LOC105378797
    nsv3110837copy number variation1nstd145human GRCh37 chr3: 21,207,475-21,221,394 , GRCh38.p12 chr3: 21,165,983-21,179,902 LOC105376988
    nsv3112094copy number variation94nstd145human GRCh37 chr7: 133,785,285-133,797,218 , GRCh38.p12 chr7: 134,100,532-134,112,465
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3116140copy number variation45nstd145human GRCh37 chr4: 21,369,066-21,376,838 , GRCh38.p12 chr4: 21,367,443-21,375,215 KCNIP4
    nsv3115066copy number variation81nstd145human GRCh37 chr6: 19,042,250-19,049,222 , GRCh38.p12 chr6: 19,042,019-19,048,991 LOC105374958
    nsv3110401copy number variation14nstd145human GRCh37 chr5: 11,129,609-11,134,869 , GRCh38.p12 chr5: 11,129,497-11,134,757 CTNND2
    nsv3114721copy number variation40nstd145human GRCh37 chr13: 32,533,404-32,538,481 , GRCh38.p12 chr13: 31,959,267-31,964,344 EEF1DP3
    nsv3118158copy number variation1nstd145human GRCh37 chr10: 24,989,376-24,993,852 , GRCh38.p12 chr10: 24,700,447-24,704,923 ARHGAP21
    nsv3114222copy number variation54nstd145human GRCh37 chr12: 82,139,806-82,144,215 , GRCh38.p12 chr12: 81,746,027-81,750,436 PPFIA2
    nsv3113252copy number variation2nstd145human GRCh37 chr8: 40,774,871-40,779,201 , GRCh38.p12 chr8: 40,917,352-40,921,682 LOC105379389
    nsv3112692copy number variation29nstd145human GRCh37 chr3: 131,708,301-131,712,626 , GRCh38.p12 chr3: 131,989,457-131,993,782 CPNE4
    nsv3113346copy number variation33nstd145human GRCh37 chr9: 29,093,646-29,097,821 , GRCh38.p12 chr9: 29,093,648-29,097,823 LINGO2
    nsv3112110copy number variation12nstd145human GRCh37 chr4: 106,940,561-106,944,506 , GRCh38.p12 chr4: 106,019,404-106,023,349 LOC101929577
    nsv3115553copy number variation167nstd145human GRCh37 chr22: 37,143,594-37,146,950 , GRCh38.p12 chr22: 36,747,550-36,750,906 CACNG2-DT
    nsv3114447copy number variation2nstd145human GRCh37 chr4: 189,437,466-189,440,166 , GRCh38.p12 chr4: 188,516,312-188,519,012 , GRCh38.p12 chr4|NT_187545.1: 179,897-182,597 LINC01060
    nsv3112012copy number variation36nstd145human GRCh37 chr1: 106,019,944-106,022,354 , GRCh38.p12 chr1: 105,477,322-105,479,732 LOC105378881
    nsv3110734copy number variation5nstd145human GRCh37 chr22: 45,554,566-45,556,546 , GRCh38.p12 chr22: 45,158,685-45,160,665 NUP50-DT
    nsv3114860copy number variation93nstd145human GRCh37 chr7: 148,073,838-148,075,734 , GRCh38.p12 chr7: 148,376,746-148,378,642 CNTNAP2
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