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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 EFS, HNRNPC, 616 more genes
    nsv3916277copy number variation1nstd102humanPathogenic NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005 EFS, MIR208B, 600 more genes
    nsv7094491copy number variation1nstd102humanPathogenic GRCh37 chr14: 23,586,696-23,902,941 , GRCh38.p12 chr14: 23,117,487-23,433,732 EFS, SLC22A17, 21 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 EFS, LOC440181, 1998 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 EFS, BANF1P1, 1996 more genes
    nsv3899639copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456 EFS, LOC100289511, 1996 more genes
    nsv3903256copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050 EFS, DHRS7, 1946 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 EFS, SRMP2, 1929 more genes
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 EFS, CRIP1, 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 EFS, MIR656, 1918 more genes
    nsv3913204copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-49,111,245 , GRCh38 chr14: 20,043,513-48,642,042 , NCBI36 chr14: 19,581,512-48,180,995 EFS, SMARCE1P3, 635 more genes
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 EFS, CDH24, 623 more genes
    nsv4675943copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827 EFS, TRAJ36, 590 more genes
    nsv3918965copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,490,852-44,562,875 , GRCh38 chr14: 20,022,693-44,093,672 , NCBI36 chr14: 19,560,692-43,632,625 EFS, TRAJ13, 589 more genes
    nsv3912710copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,000,611-38,984,415 , NCBI36 chr14: 19,538,610-38,523,370 , GRCh37 chr14: 20,468,770-39,453,619 EFS, UBE2NP1, 553 more genes
    nsv3898685copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-34,049,214 , GRCh38.p12 chr14: 19,652,445-33,580,008 EFS, LOC105370419, 480 more genes
    nsv4349901copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,100,682-28,730,087 , GRCh38.p12 chr14: 18,324,205-28,260,881 EFS, TRAV4, 458 more genes
    nsv3898291copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-27,768,254 , GRCh38.p12 chr14: 19,652,445-27,299,048 EFS, HOMEZ, 411 more genes
    nsv3920885copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,619,308-23,911,404 , NCBI36 chr14: 19,689,148-22,981,244 , GRCh38 chr14: 20,151,149-23,442,195 EFS, SLC39A2, 294 more genes
    nsv3922265copy number variation1nstd102humanLikely pathogenic NCBI36 chr14: 19,950,586-24,557,166 , GRCh37 chr14: 20,880,746-25,487,326 , GRCh38 chr14: 20,412,587-25,018,120 EFS, ANG, 346 more genes
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