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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5935089copy number variation1nstd209human GRCh38 chr14: 46,941,699-52,127,962 , GRCh37.p13 chr14: 47,410,902-52,594,680 , RNA5SP385, 92 more genes
    nsv5510485copy number variation1nstd206human GRCh38 chr14: 51,651,709-51,652,309 , GRCh37.p13 chr14: 52,118,427-52,119,027 FRMD6, FRMD6-AS1
    nsv5317804copy number variation1nstd204human GRCh37.p13 chr14: 52,118,030-52,118,436 , GRCh38.p13 chr14: 51,651,312-51,651,718 FRMD6, FRMD6-AS1
    nsv4900000mobile element deletion1nstd200human GRCh38 chr14: 51,650,395-51,650,687 , GRCh37.p13 chr14: 52,117,113-52,117,405 FRMD6-AS1, FRMD6
    nsv4775379mobile element deletion1nstd200human GRCh37 chr14: 52,117,113-52,117,405 , GRCh38.p12 chr14: 51,650,395-51,650,687 FRMD6, FRMD6-AS1
    nsv4218878copy number variation1nstd166human GRCh37.p13 chr14: 50,724,321-53,837,159 , GRCh38.p12 chr14: 50,257,603-53,370,441 , SAV1, 60 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
    nsv3916278copy number variation1nstd102humanPathogenic GRCh38 chr14: 50,591,011-56,286,919 , GRCh37 chr14: 51,057,729-56,753,637 , NCBI36 chr14: 50,127,479-55,823,390 LOC105370507, ATG14, 98 more genes
    nsv3913833copy number variation1nstd102humanPathogenic NCBI36 chr14: 51,081,314-54,857,069 , GRCh38 chr14: 51,544,846-55,320,598 , GRCh37 chr14: 52,011,564-55,787,316 SOCS4, FRMD6, 65 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
    nsv3911178copy number variation1nstd102humanUncertain significance NCBI36 chr14: 49,627,618-51,313,793 , GRCh37 chr14: 50,557,868-52,244,043 , GRCh38 chr14: 50,091,150-51,777,325 TRIM9, LINC01599, 35 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
    nsv3903380copy number variation1nstd102humanUncertain significance GRCh37 chr14: 50,598,842-52,261,074 , GRCh38.p12 chr14: 50,132,124-51,794,356 LINC02310, RN7SL452P, 33 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
    nsv1769649short tandem repeat1nstd128human GRCh37 chr14: 52,116,643-52,116,661 , GRCh38.p12 chr14: 51,649,925-51,649,943 FRMD6, FRMD6-AS1
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