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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4681960copy number variation1nstd102humanPathogenic GRCh37 chr12: 8,608,708-8,765,363 , GRCh38.p12 chr12: 8,456,112-8,612,767 CLEC4E, AICDA, 6 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 CLEC4E, RNA5SP369, 2454 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 CLEC4E, LOH12CR2, 2452 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 CLEC4E, 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 CLEC4E, BTG1P1, 2451 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 CLEC4E, 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 CLEC4E, LOC105369667, 684 more genes
    nsv3905633copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-37,869,301 , GRCh38.p12 chr12: 64,620-37,475,499 CLEC4E, RESF1, 684 more genes
    nsv3897151copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-37,869,107 , GRCh38.p12 chr12: 64,620-37,475,305 CLEC4E, CACNA2D4, 684 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 CLEC4E, 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 CLEC4E, ENO2, 684 more genes
    nsv3901714copy number variation3nstd102humanPathogenic GRCh37 chr12: 173,786-34,835,837 , GRCh38.p12 chr12: 64,620-34,682,902 CLEC4E, 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 CLEC4E, IFT57P1, 684 more genes
    nsv3907734copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,578-34,756,150 , GRCh38.p12 chr12: 80,412-34,603,215 CLEC4E, ACRBP, 684 more genes
    nsv3914149copy number variation1nstd102humanPathogenic GRCh38 chr12: 121,255-34,603,274 , NCBI36 chr12: 100,682-34,647,476 , GRCh37 chr12: 282,465-34,756,209 CLEC4E, PSMC1P8, 683 more genes
    nsv3916135copy number variation1nstd102humanPathogenic GRCh38 chr12: 121,271-34,603,261 , NCBI36 chr12: 100,698-34,647,463 , GRCh37 chr12: 282,465-34,756,196 CLEC4E, TAS2R7, 683 more genes
    nsv3916538copy number variation1nstd102humanPathogenic GRCh38 chr12: 77,187-34,380,176 , GRCh37 chr12: 282,465-34,533,111 , NCBI36 chr12: 56,614-34,424,378 CLEC4E, A2M, 684 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 CLEC4E, EMP1, 684 more genes
    nsv3906723copy number variation1nstd102humanPathogenic GRCh37 chr12: 148,034-34,178,799 , GRCh38.p12 chr12: 45,740-34,025,864 CLEC4E, LOC105369622, 680 more genes
    nsv3906484copy number variation1nstd102humanPathogenic GRCh37 chr12: 89,061-34,178,799 , GRCh38.p12 chr12: 45,740-34,025,864 CLEC4E, RN7SKP262, 680 more genes
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