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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935089copy number variation1nstd209human GRCh38 chr14: 46,941,699-52,127,962 , GRCh37.p13 chr14: 47,410,902-52,594,680 , RNA5SP385, 92 more genes
    nsv4999296copy number variation1nstd200human GRCh38 chr14: 49,615,560-49,616,598 , GRCh37.p13 chr14: 50,082,278-50,083,316 RPL36AL
    nsv4633184copy number variation1nstd183human GRCh37 chr14: 50,087,241-50,100,117 , GRCh38.p12 chr14: 49,620,523-49,633,399 DNAAF2, MGAT2, 1 more genes
    nsv4629838copy number variation1nstd183human GRCh37 chr14: 49,986,935-50,930,979 , GRCh38.p12 chr14: 49,520,217-50,464,261 , RNU6-189P, 37 more genes
    nsv4623203copy number variation1nstd183human GRCh37 chr14: 49,893,688-50,942,527 , GRCh38.p12 chr14: 49,426,970-50,475,809 , LOC105378179, 38 more genes
    nsv4218063copy number variation1nstd166human GRCh37.p13 chr14: 50,082,340-50,116,458 , GRCh38.p12 chr14: 49,615,622-49,649,740 , DNAAF2, 3 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 more genes
    nsv3911849copy number variation1nstd102humanLikely pathogenic NCBI36 chr14: 38,735,127-56,250,932 , GRCh37 chr14: 39,665,376-57,181,179 , GRCh38 chr14: 39,196,172-56,714,461 ARF6, BMP4, 219 more genes
    nsv3909218copy number variation1nstd102humanUncertain significance GRCh37 chr14: 50,073,908-50,127,672 , GRCh38.p12 chr14: 49,607,190-49,660,954 MGAT2, RPL36AL, 3 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 BANF1P1, IGHV1-68, 1996 more genes
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 CRIP1, GPATCH2L, 1929 more genes
    nsv3903256copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050 DHRS7, MIR548Y, 1946 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 LOC440181, HEATR5A-DT, 1998 more genes
    nsv3902764copy number variation1nstd102humanBenign GRCh37 chr14: 50,069,088-50,199,169 , GRCh38.p12 chr14: 49,602,370-49,732,451 POLE2, RPL36AL, 6 more genes
    nsv3899639copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456 LOC100289511, RNU6-552P, 1996 more genes
    nsv3151634copy number variation1nstd151human GRCh37 chr14: 50,044,527-50,281,580 , GRCh38.p12 chr14: 49,577,809-49,814,862 , RPL32P29, 14 more genes
    nsv2758533copy number variation1nstd130human GRCh37 chr14: 50,065,359-50,161,828 , GRCh38.p12 chr14: 49,598,641-49,695,110 , KLHDC1, 9 more genes
    nsv1769269short tandem repeat4nstd128human GRCh37 chr14: 50,084,663-50,084,677 , GRCh38.p12 chr14: 49,617,945-49,617,959 , RPL36AL
    nsv1740552short tandem repeat3nstd128human GRCh37 chr14: 50,086,349-50,086,360 , GRCh38.p12 chr14: 49,619,631-49,619,642 MGAT2, RPL36AL
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