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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6310446copy number variation1nstd102humanPathogenic GRCh37 chr19: 13,001,426-13,004,353 , GRCh38.p12 chr19: 12,890,612-12,893,539 GCDH, RPS6P25
    nsv7095470copy number variation1nstd102humanPathogenic GRCh37 chr19: 13,001,933-13,004,477 , GRCh38.p12 chr19: 12,891,119-12,893,663 GCDH, RPS6P25
    nsv7095638copy number variation1nstd102humanPathogenic GRCh37 chr19: 13,001,933-13,003,258 , GRCh38.p12 chr19: 12,891,119-12,892,444 GCDH, RPS6P25
    nsv5673302copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 13,004,287-13,004,477 , GRCh38.p12 chr19: 12,893,473-12,893,663 GCDH, RPS6P25
    nsv6314688copy number variation1nstd102humanLikely benign GRCh37 chr19: 13,004,474-13,004,533 , GRCh38 chr19: 12,893,660-12,893,719 GCDH, RPS6P25
    nsv3903242copy number variation1nstd102humanBenign GRCh37 chr19: 13,006,740-13,007,077 , GRCh38.p12 chr19: 12,895,926-12,896,263 GCDH, SYCE2
    nsv3896417copy number variation1nstd102humanBenign/Likely benign GRCh37 chr19: 13,006,847-13,007,077 , GRCh38.p12 chr19: 12,896,033-12,896,263 GCDH, SYCE2
    nsv6310618copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,996,012-13,004,373 , GRCh38.p12 chr19: 12,885,198-12,893,559 GCDH, RPS6P25, 1 more genes
    nsv6310282copy number variation1nstd102humanPathogenic GRCh37 chr19: 13,004,287-13,008,687 , GRCh38.p12 chr19: 12,893,473-12,897,873 GCDH, SYCE2, 1 more genes
    nsv4683135copy number variation1nstd102humanPathogenic GRCh37 chr19: 13,004,385-13,008,073 , GRCh38 chr19: 12,893,571-12,897,259 GCDH, SYCE2, 1 more genes
    nsv3922964copy number variation1nstd102humanPathogenic GRCh38 chr19: 10,319,474-13,777,860 , NCBI36 chr19: 10,291,150-13,749,674 , GRCh37 chr19: 10,430,150-13,888,674 GCDH, SWSAP1, 164 more genes
    nsv3922999copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,240,071-12,946,266 , GRCh37.p13 chr19: 10,379,071-13,085,266 , GRCh38.p12 chr19: 10,268,395-12,974,452 GCDH, ZNF433, 155 more genes
    nsv3924466copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,496,978-14,126,833 , GRCh38 chr19: 11,525,163-14,155,021 , GRCh37 chr19: 11,635,978-14,265,833 GCDH, JUNB, 135 more genes
    nsv3912480copy number variation1nstd102humanPathogenic GRCh38 chr19: 12,580,427-14,742,673 , GRCh37 chr19: 12,691,241-14,853,485 , NCBI36 chr19: 12,552,241-14,714,485 GCDH, GET3, 100 more genes
    nsv3907864copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,574,343-14,726,197 , GRCh38.p12 chr19: 12,463,529-14,615,385 GCDH, WDR83, 105 more genes
    nsv3919036copy number variation1nstd102humanPathogenic GRCh37 chr19: 11,628,640-13,336,101 , NCBI36 chr19: 11,489,640-13,197,101 , GRCh38 chr19: 11,517,825-13,225,287 GCDH, ZNF763, 105 more genes
    nsv6291633copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,697,728-14,111,313 , GRCh38.p12 chr19: 12,586,914-14,000,501 GCDH, RN7SL619P, 67 more genes
    nsv3907118copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,204,632-13,497,073 , GRCh38.p12 chr19: 12,093,817-13,386,259 GCDH, ZNF625, 73 more genes
    nsv4457524copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,354,642-13,424,014 , GRCh38.p12 chr19: 12,243,827-13,313,200 GCDH, BEST2, 64 more genes
    nsv6310462copy number variation2nstd102humanPathogenic GRCh37 chr19: 12,757,434-13,617,038 , GRCh38.p12 chr19: 12,646,620-13,506,224 GCDH, DHPS, 42 more genes
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