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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5496078copy number variation1nstd206human GRCh38 chr14: 22,686,736-22,843,154 , GRCh37.p13 chr14: 23,155,945-23,312,363 MMP14, OXA1L, 6 more genes
    nsv5040740inversion1nstd200human GRCh38 chr14: 22,785,016-22,863,914 , GRCh37.p13 chr14: 23,254,225-23,333,123 MMP14, SLC7A7, 1 more genes
    nsv4685750copy number variation1nstd102humannot provided GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685 IGBP1P1, RAB2B, 579 more genes
    nsv4676085copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,143,933-23,297,667 , GRCh38.p12 chr14: 20,675,774-22,828,458 ANG, SNORD8, 209 more genes
    nsv4675943copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827 TRAJ36, SEC23A-AS1, 590 more genes
    nsv4621446copy number variation1nstd183human GRCh37 chr14: 22,849,194-23,348,952 , GRCh38.p12 chr14: 22,380,791-22,879,743 , TRDV3, 89 more genes
    nsv4578270copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 21,717,093-24,027,220 , GRCh38.p12 chr14: 21,248,934-23,558,011 BCL2L2, CEBPE, 215 more genes
    nsv4422703copy number variation1nstd174human GRCh37 chr14: 23,098,218-23,312,307 , GRCh38.p12 chr14: 22,629,313-22,843,098 , MRPL52, 8 more genes
    nsv4349901copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,100,682-28,730,087 , GRCh38.p12 chr14: 18,324,205-28,260,881 TRAV4, UNGP2, 458 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 ANG, APEX1, 346 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 SLC39A2, APEX1, 294 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
    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 TRAJ13, LRP10, 589 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
    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 MIR208B, MRPL52, 600 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 SMARCE1P3, LOC100421646, 635 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 UBE2NP1, MIR4307HG, 553 more genes
    nsv3912402copy number variation1nstd102humanUncertain significance GRCh38 chr14: 21,010,790-22,951,814 , GRCh37 chr14: 21,478,949-23,421,023 , NCBI36 chr14: 20,548,789-22,490,863 TRAJ42, TRAJ19, 195 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
    nsv3904628copy number variation1nstd102humanUncertain significance GRCh37 chr14: 23,240,787-23,468,899 , GRCh38.p12 chr14: 22,771,578-22,999,690 PRMT5-DT, SLC7A7, 14 more genes
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