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Items: 1 to 20 of 2271

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944925copy number variation1nstd209human GRCh38 chr14: 22,423,043-22,449,111 , GRCh37.p13 chr14: 22,892,034-22,918,103 TRA, TRD, 6 more genes
    nsv5937530copy number variation1nstd209human GRCh38 chr14: 22,439,005-22,449,123 , GRCh37.p13 chr14: 22,907,997-22,918,115 TRA, TRD, 5 more genes
    nsv5931513copy number variation1nstd209human GRCh38 chr14: 22,314,917-22,449,111 , GRCh37.p13 chr14: 22,783,349-22,918,103 TRAV40, TRA, 9 more genes
    nsv5929180copy number variation1nstd209human GRCh38 chr14: 22,439,013-22,450,062 , GRCh37.p13 chr14: 22,908,005-22,919,054 TRA, TRD, 5 more genes
    nsv5863017copy number variation1nstd209human GRCh38 chr14: 22,438,996-22,448,745 , GRCh37.p13 chr14: 22,907,988-22,917,737 TRA, TRD, 5 more genes
    nsv5849711copy number variation1nstd209human GRCh38 chr14: 22,428,558-22,437,995 , GRCh37.p13 chr14: 22,897,551-22,906,987 TRD, TRDD1, 3 more genes
    nsv5511519copy number variation1nstd206human GRCh38 chr14: 22,438,986-22,449,136 , GRCh37.p13 chr14: 22,907,978-22,918,128 TRA, TRD, 5 more genes
    nsv5339403translocation1nstd200human GRCh38.p12 chr14: 22,449,112-22,449,112 , GRCh38.p12 chr14: 22,439,012-22,439,012 , GRCh37 chr14: 22,908,004-22,908,004 , GRCh37 chr14: 22,918,104-22,918,104 TRA, TRD, 5 more genes
    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
    nsv5263186copy number variation1nstd204human GRCh38.p13 chr14: 22,418,401-22,460,000 , GRCh37.p13 chr14: 22,887,391-22,928,992 TRDJ2, TRDD1, 9 more genes
    nsv4990799copy number variation1nstd200human GRCh38 chr14: 22,369,868-22,505,585 , GRCh37.p13 chr14: 22,838,273-22,974,572 , TRAJ54, 39 more genes
    nsv4990786copy number variation1nstd200human GRCh38 chr14: 22,124,282-22,513,938 , GRCh37.p13 chr14: 22,592,240-22,982,920 , TRDD1, 67 more genes
    nsv4846912copy number variation1nstd200human GRCh37 chr14: 22,838,273-22,974,572 , GRCh38.p12 chr14: 22,369,868-22,505,585 , TRDC, 39 more genes
    nsv4836580copy number variation1nstd200human GRCh37 chr14: 22,855,224-22,944,309 , GRCh38.p12 chr14: 22,386,821-22,475,319 , TRA, 15 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
    nsv4728120copy number variation8nstd197human GRCh38.p12 chr14: 21,941,185-22,506,702 , GRCh37 chr14: 22,409,370-22,975,687 , TRA, 78 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
    nsv4680172copy number variation1nstd189human GRCh37.p13 chr14: 22,893,640-23,020,319 , GRCh38.p12 chr14: 22,424,649-22,551,374 , TRA, 73 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
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