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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935211copy number variation1nstd209human GRCh38 chr14: 49,880,266-49,891,913 , GRCh37.p13 chr14: 50,346,984-50,358,631 ARF6
    nsv5935089copy number variation1nstd209human GRCh38 chr14: 46,941,699-52,127,962 , GRCh37.p13 chr14: 47,410,902-52,594,680 , RNA5SP385, 92 more genes
    nsv5863887copy number variation1nstd209human GRCh38 chr14: 49,880,943-49,891,392 , GRCh37.p13 chr14: 50,347,661-50,358,110 ARF6
    nsv5279497copy number variation1nstd204human GRCh37.p13 chr14: 50,192,319-50,379,318 , GRCh38.p13 chr14: 49,725,601-49,912,600 ARF6, NEMF, 7 more genes
    nsv4675996copy number variation1nstd102humanUncertain significance GRCh37 chr14: 50,317,272-51,627,752 , GRCh38.p12 chr14: 49,850,554-51,161,034 TRIM9, LINC01588, 32 more genes
    nsv4632655copy number variation1nstd183human GRCh37 chr14: 50,198,095-51,541,608 , GRCh38.p12 chr14: 49,731,377-51,074,890 , ABHD12B, 37 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
    nsv4375601copy number variation1nstd173human GRCh37 chr14: 50,337,754-50,386,980 , GRCh38.p12 chr14: 49,871,036-49,920,262 ARF6, LOC100506446, 1 more genes
    nsv4222381copy number variation1nstd166human GRCh37.p13 chr14: 50,362,992-50,363,044 , GRCh38.p12 chr14: 49,896,274-49,896,326 ARF6
    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
    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
    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
    nsv3145659copy number variation1nstd151human GRCh37 chr14: 50,301,078-50,360,987 , GRCh38.p12 chr14: 49,834,360-49,894,269 RN7SL3, NEMF, 4 more genes
    nsv1740615short tandem repeat3nstd128human GRCh37 chr14: 50,359,301-50,359,319 , GRCh38.p12 chr14: 49,892,583-49,892,601 ARF6
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