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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv442545copy number variation121nstd22human NCBI35 chr9: 43,806,624-43,934,502 , GRCh37.p13 chr9: 44,727,859-44,855,737 , GRCh38.p12 chr9: 61,520,021-61,647,899 LOC105379437
    nsv442532copy number variation6nstd22human NCBI35 chr8: 137,836,926-137,925,499 , GRCh37.p13 chr8: 137,767,744-137,856,317 , GRCh38.p12 chr8: 136,755,501-136,844,074 LINC02055
    nsv442779copy number variation41nstd22human NCBI35 chr20: 28,034,013-28,119,552 , GRCh37.p13 chr20: 29,420,352-29,505,891 , GRCh38.p12 chr20: 30,185,676-30,271,215 CFTRP3
    nsv442991copy number variation65nstd22human NCBI35 chr6: 79,025,784-79,091,904 , GRCh37.p13 chr6: 78,969,065-79,035,185 , GRCh38.p12 chr6: 78,259,348-78,325,468 LOC105377865
    nsv442908copy number variation238nstd22human NCBI35 chr1: 72,480,937-72,523,169 , GRCh37.p13 chr1: 72,768,916-72,811,148 , GRCh38.p12 chr1: 72,303,233-72,345,465 , GRCh38.p12 chr1|NW_018654707.1: 15,500-66,690 LOC105378797
    nsv442969copy number variation206nstd22human NCBI35 chr5: 177,090,005-177,131,055 , GRCh37.p13 chr5: 177,157,399-177,198,449 , GRCh38.p12 chr5: 177,730,398-177,771,448 FAM153A
    nsv442601copy number variation72nstd22human NCBI35 chr11: 7,769,616-7,798,159 , GRCh37.p13 chr11: 7,813,040-7,841,583 , GRCh38.p12 chr11: 7,791,493-7,820,036 , GRCh38.p12 chr11|NT_187583.1: 12,361-40,904 , GRCh38.p12 chr11|NW_011332695.1: 12,361-51,026 OR5P2
    nsv442776copy number variation260nstd22human NCBI35 chr20: 1,509,580-1,541,893 , GRCh37.p13 chr20: 1,561,580-1,593,893 , GRCh38.p12 chr20: 1,580,934-1,613,247 SIRPB1
    nsv442803copy number variation170nstd22human NCBI35 chr2: 97,599,265-97,620,228 , GRCh37.p13 chr2: 98,140,747-98,161,710 , GRCh38.p12 chr2: 97,524,284-97,545,247 ANKRD36B
    nsv441983copy number variation113nstd22human NCBI35 chr7: 66,073,479-66,089,382 , GRCh37.p13 chr7: 66,629,329-66,645,232 , GRCh38.p12 chr7: 67,164,342-67,180,245 TYW1
    nsv442759copy number variation270nstd22human NCBI35 chr19: 8,256,197-8,271,067 , GRCh37.p13 chr19: 8,350,197-8,365,067 , GRCh38.p12 chr19: 8,285,313-8,300,183 CD320
    nsv442294copy number variation267nstd22human NCBI35 chr7: 157,617,027-157,631,641 , GRCh37.p13 chr7: 158,117,551-158,132,165 , GRCh38.p12 chr7: 158,324,859-158,339,473 , GRCh38.p12 chr7|NT_187560.1: 137,702-152,355 PTPRN2
    nsv442150copy number variation117nstd22human NCBI35 chr7: 133,242,450-133,256,409 , GRCh37.p13 chr7: 133,785,195-133,799,154 , GRCh38.p12 chr7: 134,100,442-134,114,401
    nsv442518copy number variation92nstd22human NCBI35 chr8: 58,279,104-58,292,579 , GRCh37.p13 chr8: 58,116,550-58,130,025 , GRCh38.p12 chr8: 57,203,991-57,217,466 LINC01606
    nsv442286copy number variation134nstd22human NCBI35 chr7: 156,837,843-156,850,316 , GRCh37.p13 chr7: 157,338,367-157,350,840 , GRCh38.p12 chr7: 157,545,673-157,558,146 PTPRN2
    nsv442730copy number variation99nstd22human NCBI35 chr16: 76,929,941-76,942,266 , GRCh37.p13 chr16: 78,372,440-78,384,765 , GRCh38.p12 chr16: 78,338,543-78,350,868 WWOX
    nsv442587copy number variation165nstd22human NCBI35 chr10: 81,475,459-81,486,935 , GRCh37.p13 chr10: 81,485,267-81,496,755 , GRCh38.p12 chr10: 79,725,511-79,736,999 NUTM2B-AS1
    nsv442936copy number variation91nstd22human NCBI35 chr5: 12,868,780-12,879,650 , GRCh37.p13 chr5: 12,815,780-12,826,650 , GRCh38.p12 chr5: 12,815,668-12,826,538 LOC105374657
    nsv442578copy number variation72nstd22human NCBI35 chr10: 56,353,096-56,362,605 , GRCh37.p13 chr10: 56,683,090-56,692,599 , GRCh38.p12 chr10: 54,923,330-54,932,839 PCDH15
    nsv442782copy number variation156nstd22human NCBI35 chr2: 87,426,037-87,434,600 , GRCh37.p13 chr2: 87,514,379-87,522,942 , GRCh38.p12 chr2: 87,287,256-87,295,819 LOC107985908
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