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Items: 1 to 20 of 1835

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5279501copy number variation1nstd204human GRCh38.p13 chr14: 21,979,101-22,279,400 , GRCh37.p13 chr14: 22,447,341-22,747,283 TRAV33, TRAV30, 28 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
    nsv5278024copy number variation1nstd204human GRCh38.p13 chr14: 22,144,701-22,230,200 , GRCh37.p13 chr14: 22,612,655-22,698,087 TRAV36DV7, TRAV30, 10 more genes
    nsv5265190copy number variation1nstd204human GRCh38.p13 chr14: 22,110,601-22,302,800 , GRCh37.p13 chr14: 22,578,807-22,770,690 TRAV8-7, TRAV39, 18 more genes
    nsv5261285copy number variation1nstd204human GRCh38.p13 chr14: 22,200,701-22,306,800 , GRCh37.p13 chr14: 22,668,595-22,774,686 TRAV37, TRAV34, 8 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
    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
    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
    nsv4668296copy number variation1nstd186human GRCh37 chr14: 22,549,069-22,959,340 , GRCh38.p12 chr14: 22,080,807-22,490,352 , TRAV37, 51 more genes
    nsv4633263copy number variation2nstd183human GRCh37 chr14: 22,549,069-22,959,340 , GRCh38.p12 chr14: 22,080,807-22,490,352 , TRAV29DV5, 51 more genes
    nsv4633043copy number variation1nstd183human GRCh37 chr14: 22,681,025-22,704,238 , GRCh38.p12 chr14: 22,213,119-22,236,357 TRAV36DV7, TRA, 1 more genes
    nsv4631105copy number variation2nstd183human GRCh37 chr14: 22,595,672-22,776,172 , GRCh38.p12 chr14: 22,127,715-22,307,753 TRA, TRAV38-1, 16 more genes
    nsv4629401copy number variation1nstd183human GRCh37 chr14: 22,677,776-22,724,111 , GRCh38.p12 chr14: 22,209,880-22,256,227 TRAV36DV7, TRA, 1 more genes
    nsv4629094copy number variation1nstd183human GRCh37 chr14: 22,614,896-22,745,625 , GRCh38.p12 chr14: 22,146,942-22,277,742 TRAV38-1, TRAV30, 12 more genes
    nsv4619643copy number variation2nstd183human GRCh37 chr14: 22,478,446-22,969,877 , GRCh38.p12 chr14: 22,010,207-22,500,894 , TRAJ45, 65 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
    nsv4428249copy number variation1nstd174human GRCh37 chr14: 22,553,002-22,804,704 , GRCh38.p12 chr14: 22,084,726-22,336,275 TRAV31, TRAV26-1, 24 more genes
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