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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4455433copy number variation1nstd102humanUncertain significance GRCh37 chr12: 8,966,269-8,986,611 , GRCh38.p12 chr12: 8,813,673-8,834,015 A2ML1
    nsv7094227copy number variation1nstd102humanUncertain significance GRCh37 chr12: 8,975,248-8,991,838 , GRCh38.p12 chr12: 8,822,652-8,839,242 A2ML1
    nsv7093982copy number variation1nstd102humanUncertain significance GRCh37 chr12: 9,000,125-9,007,447 , GRCh38.p12 chr12: 8,847,529-8,854,851 A2ML1
    nsv4453260copy number variation1nstd102humanUncertain significance GRCh38 chr12: 8,857,487-8,861,317 , GRCh37 chr12: 9,010,083-9,013,913 A2ML1
    nsv4450478copy number variation1nstd102humanUncertain significance GRCh38 chr12: 8,857,497-8,861,307 , GRCh37 chr12: 9,010,093-9,013,903 A2ML1
    nsv7094057copy number variation1nstd102humanUncertain significance GRCh37 chr12: 8,975,248-8,976,498 , GRCh38.p12 chr12: 8,822,652-8,823,902 A2ML1
    nsv4681224copy number variation1nstd102humanUncertain significance GRCh37 chr12: 8,975,228-9,027,627 , GRCh38.p12 chr12: 8,822,632-8,875,031 A2ML1
    nsv7094058copy number variation1nstd102humanUncertain significance GRCh37 chr12: 8,995,710-9,027,607 , GRCh38.p12 chr12: 8,843,114-8,875,011 A2ML1
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 A2ML1, RNA5SP369, 2454 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 A2ML1, LOH12CR2, 2452 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 A2ML1, RNU4ATAC16P, 2452 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 A2ML1, BTG1P1, 2451 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 A2ML1, OR5BT1P, 2441 more genes
    nsv3914427copy number variation1nstd102humanPathogenic NCBI36 chr12: 18,636-36,150,744 , GRCh37.p13 chr12: 148,375-37,864,477 , GRCh38.p12 chr12: 43,334-37,470,675 A2ML1, LOC105369667, 684 more genes
    nsv3905633copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-37,869,301 , GRCh38.p12 chr12: 64,620-37,475,499 A2ML1, RESF1, 684 more genes
    nsv3897151copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-37,869,107 , GRCh38.p12 chr12: 64,620-37,475,305 A2ML1, CACNA2D4, 684 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 A2ML1, LOC105376675, 682 more genes
    nsv3924262copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,835,837 , GRCh38 chr12: 64,620-34,682,902 , NCBI36 chr12: 44,047-34,727,104 A2ML1, ENO2, 684 more genes
    nsv3901714copy number variation3nstd102humanPathogenic GRCh37 chr12: 173,786-34,835,837 , GRCh38.p12 chr12: 64,620-34,682,902 A2ML1, LOC105369677, 684 more genes
    nsv3911928copy number variation1nstd102humanPathogenic GRCh37 chr12: 282,465-34,761,006 , GRCh38 chr12: 54,427-34,608,071 , NCBI36 chr12: 33,854-34,652,273 A2ML1, IFT57P1, 684 more genes
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