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Items: 1 to 20 of 71

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094491copy number variation1nstd102humanPathogenic GRCh37 chr14: 23,586,696-23,902,941 , GRCh38.p12 chr14: 23,117,487-23,433,732 SLC22A17, CMTM5, 21 more genes
    nsv7094423copy number variation2nstd102humanUncertain significance GRCh37 chr14: 23,242,819-25,103,366 , GRCh38.p12 chr14: 22,773,610-24,634,160 LINC00596, NGDN, 107 more genes
    nsv7074310inversion1nstd229human GRCh38 chr14: 22,076,285-27,854,954 , GRCh37.p13 chr14: 22,544,546-28,324,160 PPP1R3E, TRAJ37, 242 more genes
    nsv6956924copy number variation1nstd229human GRCh38 chr14: 23,354,601-23,354,824 , GRCh37.p13 chr14: 23,823,810-23,824,033 SLC22A17, EFS
    nsv6952014copy number variation1nstd229human GRCh38 chr14: 23,247,096-23,376,847 , GRCh37.p13 chr14: 23,716,305-23,846,056 HOMEZ, RNU6-1046P, 11 more genes
    nsv6945698copy number variation1nstd229human GRCh38 chr14: 23,281,701-23,431,900 , GRCh37.p13 chr14: 23,750,910-23,901,109 BCL2L2, SLC22A17, 13 more genes
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv6313998copy number variation1nstd102humanUncertain significance GRCh37 chr14: 23,590,841-23,823,265 , GRCh38.p12 chr14: 23,121,632-23,354,056 SLC7A8, PPP1R3E, 12 more genes
    nsv6132862copy number variation1nstd213human GRCh37 chr14: 23,180,000-23,940,001 , GRCh38.p12 chr14: 22,710,791-23,470,792 BCL2L2, CEBPE, 47 more genes
    nsv6132775copy number variation1nstd213human GRCh37 chr14: 22,590,000-24,410,001 , GRCh38.p12 chr14: 22,122,042-23,940,792 BCL2L2, CEBPE, 167 more genes
    nsv4994112copy number variation1nstd200human GRCh38 chr14: 23,335,826-23,345,225 , GRCh37.p13 chr14: 23,805,035-23,814,434 SLC22A17
    nsv4990860copy number variation1nstd200human GRCh38 chr14: 23,335,741-23,344,901 , GRCh37.p13 chr14: 23,804,950-23,814,110 SLC22A17
    nsv4843396copy number variation1nstd200human GRCh37 chr14: 23,804,950-23,814,110 , GRCh38.p12 chr14: 23,335,741-23,344,901 SLC22A17
    nsv4834954copy number variation1nstd200human GRCh37 chr14: 23,805,035-23,814,434 , GRCh38.p12 chr14: 23,335,826-23,345,225 SLC22A17
    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
    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
    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
    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
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