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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3116050copy number variation42nstd145human GRCh37 chr14: 41,610,263-41,668,279 , GRCh38.p12 chr14: 41,141,060-41,199,076 LINC02315
    nsv3117146copy number variation1nstd145human GRCh37 chr11: 97,822,616-97,876,272 , GRCh38.p12 chr11: 97,951,616-98,005,544 LINC02713
    nsv3118081copy number variation72nstd145human GRCh37 chr7: 141,766,533-141,793,377 , GRCh38.p12 chr7|NT_187562.1: 28,613-55,457 , GRCh38.p12 chr7: 142,066,733-142,093,577 MGAM
    nsv3111947copy number variation1nstd145human GRCh37 chr6: 169,251,050-169,267,375 , GRCh38.p12 chr6: 168,850,955-168,867,280 , GRCh38.p12 chr6|NW_004166862.2: 85,132-101,457 LOC105378144
    nsv3112771copy number variation10nstd145human GRCh37 chr5: 114,706,231-114,721,117 , GRCh38.p12 chr5: 115,370,534-115,385,420 LOC105379130
    nsv3113357copy number variation1nstd145human GRCh37 chr18: 66,745,402-66,759,255 , GRCh38.p12 chr18: 69,078,165-69,092,018 CCDC102B
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3111733copy number variation53nstd145human GRCh37 chr1: 169,227,837-169,240,805 , GRCh38.p12 chr1: 169,258,599-169,271,567 NME7
    nsv3113383copy number variation199nstd145human GRCh37 chr3: 192,875,554-192,885,008 , GRCh38.p12 chr3: 193,157,765-193,167,219 VEZF1P1
    nsv3116850copy number variation4nstd145human GRCh37 chr17: 50,117,176-50,126,228 , GRCh38.p12 chr17: 52,039,816-52,048,868 CA10
    nsv3110942copy number variation60nstd145human GRCh37 chr7: 91,033,585-91,042,496 , GRCh38.p12 chr7: 91,404,270-91,413,181 LINC02932
    nsv3110366copy number variation1nstd145human GRCh37 chr7: 81,921,588-81,929,627 , GRCh38.p12 chr7: 82,292,272-82,300,311 CACNA2D1
    nsv3117540copy number variation1nstd145human GRCh37 chr1: 72,793,267-72,799,854 , GRCh38.p12 chr1: 72,327,584-72,334,171 , GRCh38.p12 chr1|NW_018654707.1: 39,851-46,438 LOC105378797
    nsv3114721copy number variation40nstd145human GRCh37 chr13: 32,533,404-32,538,481 , GRCh38.p12 chr13: 31,959,267-31,964,344 EEF1DP3
    nsv3114178copy number variation107nstd145human GRCh37 chr6: 53,928,991-53,933,879 , GRCh38.p12 chr6: 54,064,193-54,069,081 MLIP
    nsv3115871copy number variation21nstd145human GRCh37 chr11: 99,647,381-99,652,155 , GRCh38.p12 chr11: 99,776,650-99,781,424 CNTN5
    nsv3114222copy number variation54nstd145human GRCh37 chr12: 82,139,806-82,144,215 , GRCh38.p12 chr12: 81,746,027-81,750,436 PPFIA2
    nsv3113215copy number variation1nstd145human GRCh37 chr1: 234,315,733-234,319,916 , GRCh38.p12 chr1: 234,179,987-234,184,170 , GRCh38.p12 chr1|NT_187521.1: 16,531-20,714 SLC35F3
    nsv3111612copy number variation21nstd145human GRCh37 chr8: 3,786,042-3,790,180 , GRCh38.p12 chr8: 3,928,520-3,932,658 CSMD1
    nsv3112046copy number variation55nstd145human GRCh37 chr19: 54,556,015-54,560,055 , GRCh38.p12 chr19: 54,052,761-54,056,801 , GRCh38.p12 chr19|NT_187693.1: 27,128-31,168 , GRCh38.p12 chr19|NW_003571061.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571057.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571058.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571059.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571060.1: 27,128-31,168 , GRCh38.p12 chr19|NW_003571056.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571055.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571054.1: 27,128-31,168 VSTM1
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