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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
    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
    nsv442683copy number variation57nstd22human NCBI35 chr14: 40,680,246-40,727,099 , GRCh37.p13 chr14: 41,610,496-41,657,349 , GRCh38.p12 chr14: 41,141,293-41,188,146 LINC02315
    nsv442612copy number variation29nstd22human NCBI35 chr11: 49,667,437-49,714,078 , GRCh37.p13 chr11: 49,710,861-49,757,502 , GRCh38.p12 chr11: 49,689,309-49,735,950 , GRCh38.p12 chr11|NW_019805495.1: 153,491-200,099 GRM5P1
    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
    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
    nsv442723copy number variation78nstd22human NCBI35 chr16: 54,353,890-54,379,945 , GRCh37.p13 chr16: 55,796,389-55,822,444 , GRCh38.p12 chr16: 55,762,477-55,788,532 CES1P1
    nsv442187copy number variation52nstd22human NCBI35 chr7: 141,222,827-141,245,092 , GRCh37.p13 chr7|NW_003571040.1: 211,794-234,059 , GRCh37.p13 chr7: 141,769,643-141,791,908 , GRCh38.p12 chr7: 142,069,843-142,092,108 , GRCh38.p12 chr7|NT_187562.1: 31,723-53,988 MGAM
    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
    nsv442671copy number variation119nstd22human NCBI35 chr13: 56,656,271-56,676,381 , GRCh37.p13 chr13: 57,758,270-57,778,380 , GRCh38.p12 chr13: 57,184,136-57,204,246 MTCO2P3
    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
    nsv442860copy number variation20nstd22human NCBI35 chr3: 53,003,416-53,016,559 , GRCh37.p13 chr3: 53,028,376-53,041,519 , GRCh38.p12 chr3: 52,994,360-53,007,503 SFMBT1
    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
    nsv442840copy number variation103nstd22human NCBI35 chr2: 179,892,698-179,904,650 , GRCh37.p13 chr2: 180,067,192-180,079,144 , GRCh38.p12 chr2: 179,202,465-179,214,417 SESTD1
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