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    Number of Variants: 10

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6310503copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,429,206-8,455,360 , GRCh38.p12 chr19: 8,364,322-8,390,476 ANGPTL4, RAB11B-AS1, 2 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ANGPTL4, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 ANGPTL4, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 ANGPTL4, LENG8, 2408 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 ANGPTL4, SEMA6B, 299 more genes
    nsv3890584copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144 ANGPTL4, PCP2, 250 more genes
    nsv3888397copy number variation1nstd102humanLikely pathogenic GRCh38 chr19: 7,981,357-10,019,383 , GRCh37.p13 chr19: 8,046,241-10,130,059 ANGPTL4, ELAVL1, 80 more genes
    nsv7095676copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,586,521-8,670,595 , GRCh38.p12 chr19: 7,521,635-8,605,710 ANGPTL4, LRRC8E, 53 more genes
    nsv4676269copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,657,490-8,569,762 , GRCh38.p12 chr19: 7,592,604-8,504,878 ANGPTL4, LRRC8E, 47 more genes
    nsv3921240copy number variation1nstd102humanUncertain significance NCBI36 chr19: 8,025,412-8,572,615 , GRCh37.p13 chr19: 8,119,412-8,666,615 , GRCh38.p12 chr19: 8,054,528-8,601,731 ANGPTL4, ADAMTS10, 18 more genes
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