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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5500308copy number variation1nstd206human GRCh38 chr14: 21,793,610-21,831,268 , GRCh37.p13 chr14: 22,261,781-22,299,424 TRA, TRAV10, 3 more genes
    nsv4994094copy number variation1nstd200human GRCh38 chr14: 21,778,204-21,852,216 , GRCh37.p13 chr14: 22,246,423-22,320,393 TRAV12-1, TRAV8-3, 7 more genes
    nsv4846760copy number variation1nstd200human GRCh37 chr14: 22,246,423-22,320,393 , GRCh38.p12 chr14: 21,778,204-21,852,216 TRA, TRAV10, 7 more genes
    nsv4728411copy number variation1nstd102humanUncertain significance GRCh37 chr14: 22,006,109-23,241,448 , GRCh38.p12 chr14: 21,537,975-22,772,239 OR4E2, TRAV10, 152 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
    nsv4633729copy number variation1nstd183human GRCh37 chr14: 22,229,021-22,354,103 , GRCh38.p12 chr14: 21,760,737-21,885,921 TRAV8-3, TRAV13-1, 9 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
    nsv4530716copy number variation1nstd166human GRCh37.p13 chr14: 22,203,999-22,380,000 , GRCh38.p12 chr14: 21,735,717-21,911,826 TRAV7, TRAV12-2, 15 more genes
    nsv4504241mobile element insertion1nstd166human GRCh37.p13 chr14: 22,278,910-22,278,910 , GRCh38.p12 chr14: 21,810,738-21,810,738 TRA, TRAV9-1
    nsv4455618copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,678,344-22,299,981 , GRCh38.p12 chr14: 21,210,185-21,831,825 TRAV3, RBBP4P5, 36 more genes
    nsv4365363copy number variation1nstd173human GRCh37 chr14: 22,033,010-22,562,282 , GRCh38.p12 chr14: 21,564,879-22,094,005 , TRAV5, 44 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
    nsv4223465copy number variation1nstd166human GRCh37.p13 chr14: 22,273,689-22,404,030 , GRCh38.p12 chr14: 21,805,517-21,935,856 TRAV14DV4, TRAV9-1, 11 more genes
    nsv4223209copy number variation1nstd166human GRCh37.p13 chr14: 22,095,569-22,713,973 , GRCh38.p12 chr14: 21,627,416-22,246,089 , TRAV8-5, 54 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
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