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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3882035copy number variation1nstd102humanPathogenic GRCh37 chr4: 93,978,239-94,073,948 , GRCh38.p12 chr4: 93,057,088-93,152,797 GRID2
    nsv7098694copy number variation1nstd102humanPathogenic GRCh38 chr7: 146,774,271-146,839,904 , GRCh37.p13 chr7: 146,471,363-146,536,996 CNTNAP2
    nsv3894893copy number variation1nstd102humanPathogenic GRCh37 chr16: 78,180,603-78,208,482 , GRCh38.p12 chr16: 78,146,706-78,174,585 WWOX
    nsv7098848copy number variation1nstd102humanPathogenic GRCh38 chr10: 72,138,925-72,163,147 , GRCh37.p13 chr10: 73,898,683-73,922,905 ASCC1
    nsv3920070copy number variation2nstd102humanPathogenic, Pathogenic/Likely pathogenic GRCh37 chr7: 80,256,737-80,280,613 , NCBI36 chr7: 80,094,673-80,118,549 , GRCh38 chr7: 80,627,421-80,651,297 CD36
    nsv4350189copy number variation1nstd102humanPathogenic GRCh37 chr16: 78,409,180-78,431,277 , GRCh38.p12 chr16: 78,375,283-78,397,380 WWOX
    nsv4350375copy number variation1nstd102humanPathogenic GRCh37 chr16: 78,143,268-78,154,701 , GRCh38.p12 chr16: 78,109,371-78,120,804 WWOX
    nsv7137081copy number variation1nstd102humanPathogenic GRCh37 chr15: 53,956,695-53,960,388 , GRCh38 chr15: 53,664,498-53,668,191 WDR72
    nsv6290194copy number variation1nstd102humanPathogenic GRCh37 chr3: 128,779,622-128,781,249 , GRCh38 chr3: 129,060,779-129,062,406 GP9
    nsv6636025copy number variation1nstd102humanPathogenic GRCh37 chr5: 42,693,862-42,695,083 , GRCh38 chr5: 42,693,760-42,694,981 GHR
    nsv7137080copy number variation1nstd102humanPathogenic GRCh38 chr22: 50,276,656-50,277,243 , GRCh37 chr22: 50,715,085-50,715,672 PLXNB2
    nsv7098825copy number variation1nstd102humanPathogenic GRCh37 chr7: 33,303,902-33,303,986 , GRCh38 chr7: 33,264,290-33,264,374 BBS9
    nsv3916216copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 56,529,926-56,538,197 , GRCh38 chr16: 56,496,014-56,504,285 BBS2
    nsv3912767copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 73,006,570-73,014,289 , GRCh38 chr15: 72,714,229-72,721,948 BBS4
    nsv3916286copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 73,006,584-73,012,788 , GRCh38 chr15: 72,714,243-72,720,447 BBS4
    nsv3920288copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 97,508,904-97,513,012 , GRCh38 chr3: 97,790,061-97,794,169 ARL6
    nsv3881924copy number variation1nstd102humanUncertain significance GRCh37 chr2: 148,859,098-148,990,429 , GRCh38.p12 chr2: 148,101,529-148,232,860 MBD5
    nsv7148042copy number variation1nstd102humanUncertain significance GRCh38 chr1: 12,617,574-12,621,498 , GRCh37.p13 chr1: 12,677,580-12,681,504 DHRS3
    nsv7098691copy number variation1nstd102humanUncertain significance GRCh38 chr7: 147,977,862-147,977,989 , GRCh37.p13 chr7: 147,674,954-147,675,081 CNTNAP2
    nsv3890287copy number variation1nstd102humanUncertain significance NCBI36 chr2: 1,396,472-1,501,946 , GRCh38 chr2: 1,413,693-1,519,167 , GRCh37 chr2: 1,417,465-1,522,939 TPO
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