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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5500724copy number variation1nstd206human GRCh38 chr14: 22,612,378-22,614,974 , GRCh37.p13 chr14: 23,081,284-23,083,877 ABHD4
    nsv5349029translocation1nstd200human GRCh38 chr14: 22,612,377-22,612,377 , GRCh38 chr14: 22,614,974-22,614,974 , GRCh37.p13 chr14: 23,083,877-23,083,877 , GRCh37.p13 chr14: 23,081,283-23,081,283 ABHD4
    nsv5340613translocation1nstd200human GRCh37 chr14: 23,083,877-23,083,877 , GRCh37 chr14: 23,081,284-23,081,284 , GRCh38.p12 chr14: 22,612,378-22,612,378 , GRCh38.p12 chr14: 22,614,974-22,614,974 ABHD4
    nsv5278812copy number variation1nstd204human GRCh38.p13 chr14: 21,896,901-22,636,500 , GRCh37.p13 chr14: 22,365,081-23,105,185 , TRAV23DV6, 119 more genes
    nsv4990806copy number variation1nstd200human GRCh38 chr14: 22,603,164-22,610,016 , GRCh37.p13 chr14: 23,072,069-23,078,922 ABHD4
    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
    nsv4621446copy number variation1nstd183human GRCh37 chr14: 22,849,194-23,348,952 , GRCh38.p12 chr14: 22,380,791-22,879,743 , TRDV3, 89 more genes
    nsv4620639copy number variation1nstd183human GRCh37 chr14: 23,027,378-23,070,237 , GRCh38.p12 chr14: 22,558,476-22,601,332 DAD1, ABHD4, 1 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
    nsv4529536copy number variation1nstd166human GRCh37.p13 chr14: 22,950,998-23,140,000 , GRCh38.p12 chr14: 22,482,009-22,670,791 , TRAJ55, 63 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
    nsv4231275copy number variation1nstd166human GRCh37.p13 chr14: 23,081,284-23,083,877 , GRCh38.p12 chr14: 22,612,378-22,614,974 ABHD4
    nsv4222723copy number variation1nstd166human GRCh37.p13 chr14: 23,073,442-23,078,140 , GRCh38.p12 chr14: 22,604,537-22,609,234 ABHD4
    nsv3955787copy number variation1nstd168human GRCh38 chr14: 22,598,427-22,676,517 , GRCh37.p13 chr14: 23,067,336-23,145,726 , ABHD4, 1 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
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