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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3114599copy number variation6nstd145human GRCh37 chr9: 12,009,087-12,100,613 , GRCh38.p12 chr9: 12,009,087-12,100,613 LOC105375976
    nsv3117742copy number variation1nstd145human GRCh37 chr19: 28,485,206-28,556,873 , GRCh38.p12 chr19: 27,994,299-28,065,966 LINC02987
    nsv3111691copy number variation1nstd145human GRCh37 chr8: 39,341,866-39,360,683 , GRCh38.p12 chr8: 39,484,347-39,503,164 ADAM3A
    nsv3118198copy number variation1nstd145human GRCh37 chr1: 61,000,193-61,015,319 , GRCh38.p12 chr1: 60,534,521-60,549,647 LINC01748
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3113552copy number variation2nstd145human GRCh37 chr16: 78,371,853-78,384,061 , GRCh38.p12 chr16: 78,337,956-78,350,164 WWOX
    nsv3117616copy number variation1nstd145human GRCh37 chr3: 36,202,032-36,214,197 , GRCh38.p12 chr3: 36,160,540-36,172,705 RFC3P1
    nsv3111509copy number variation29nstd145human GRCh37 chr8: 2,150,517-2,161,441 , GRCh38.p12 chr8|NT_187576.1: 385,727-396,651 , GRCh38.p12 chr8: 2,202,878-2,213,774 LOC105377782
    nsv3112240copy number variation2nstd145human GRCh37 chr11: 7,816,612-7,826,930 , GRCh38.p12 chr11: 7,795,065-7,805,383 , GRCh38.p12 chr11|NT_187583.1: 15,933-26,251 , GRCh38.p12 chr11|NW_011332695.1: 15,933-26,251 OR5P2
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3115987copy number variation16nstd145human GRCh37 chr18: 66,749,133-66,756,183 , GRCh38.p12 chr18: 69,081,896-69,088,946 CCDC102B
    nsv3110593copy number variation88nstd145human GRCh37 chr8: 40,774,871-40,779,295 , GRCh38.p12 chr8: 40,917,352-40,921,776 LOC105379389
    nsv3110186copy number variation2nstd145human GRCh37 chr9: 28,047,215-28,050,923 , GRCh38.p12 chr9: 28,047,217-28,050,925 LINGO2
    nsv3114451copy number variation90nstd145human GRCh37 chr12: 90,487,994-90,491,654 , GRCh38.p12 chr12: 90,094,217-90,097,877 LOC105369890
    nsv3112939copy number variation3nstd145human GRCh37 chr1: 42,686,162-42,689,131 , GRCh38.p12 chr1: 42,220,491-42,223,460 FOXJ3
    nsv3111468copy number variation114nstd145human GRCh37 chr2: 33,224,481-33,227,121 , GRCh38.p12 chr2: 32,999,414-33,002,054 LTBP1
    nsv3116406copy number variation4nstd145human GRCh37 chr7: 147,282,016-147,284,647 , GRCh38.p12 chr7: 147,584,924-147,587,555 CNTNAP2
    nsv3114005copy number variation35nstd145human GRCh37 chr22: 37,144,978-37,146,950 , GRCh38.p12 chr22: 36,748,934-36,750,906 CACNG2-DT
    nsv3117458copy number variation67nstd145human GRCh37 chr5: 147,553,255-147,554,688 , GRCh38.p12 chr5: 148,173,692-148,175,125 SPINK14
    nsv3113782copy number variation53nstd145human GRCh37 chr13: 34,135,737-34,144,789 , GRCh38.p12 chr13: 33,561,600-33,570,652 STARD13, LOC102723406
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