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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5857459copy number variation1nstd209human GRCh38 chr14: 26,806,651-26,808,650 , GRCh37.p13 chr14: 27,275,857-27,277,856 LINC02294, LINC02293, 1 more genes
    nsv5512759copy number variation1nstd206human GRCh38 chr14: 26,811,477-26,860,605 , GRCh37.p13 chr14: 27,280,683-27,329,811 LINC02293, LINC02294
    nsv5511430copy number variation1nstd206human GRCh38 chr14: 26,781,303-26,811,104 , GRCh37.p13 chr14: 27,250,509-27,280,310 LINC02294, NOVA1-DT, 1 more genes
    nsv5500622copy number variation1nstd206human GRCh38 chr14: 26,807,174-26,807,446 , GRCh37.p13 chr14: 27,276,380-27,276,652 LINC02294, LINC02293
    nsv4994133copy number variation1nstd200human GRCh38 chr14: 26,811,497-26,860,585 , GRCh37.p13 chr14: 27,280,703-27,329,791 LINC02294, LINC02293
    nsv4990979copy number variation1nstd200human GRCh38 chr14: 26,781,301-26,811,105 , GRCh37.p13 chr14: 27,250,507-27,280,311 LINC02294, NOVA1-DT, 1 more genes
    nsv4990977copy number variation1nstd200human GRCh38 chr14: 26,773,152-26,909,052 , GRCh37.p13 chr14: 27,242,358-27,378,258 LINC02293, NOVA1-DT, 3 more genes
    nsv4839410copy number variation1nstd200human GRCh37 chr14: 27,250,507-27,280,311 , GRCh38.p12 chr14: 26,781,301-26,811,105 LINC02293, LINC02294, 1 more genes
    nsv4729530copy number variation1nstd102humanPathogenic GRCh37 chr14: 25,172,628-30,285,023 , GRCh38.p12 chr14: 24,703,422-29,815,817 LINC02281, RNU6-864P, 42 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
    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
    nsv4621404copy number variation2nstd183human GRCh37 chr14: 27,280,768-27,329,091 , GRCh38.p12 chr14: 26,811,562-26,859,885 LINC02294, LINC02293
    nsv4529455copy number variation1nstd166human GRCh37.p13 chr14: 26,335,999-27,430,000 , GRCh38.p12 chr14: 25,866,793-26,960,794 MIR4307, LOC105370419, 8 more genes
    nsv4419761copy number variation1nstd174human GRCh37 chr14: 27,280,572-27,330,481 , GRCh38.p12 chr14: 26,811,366-26,861,275 LINC02294, LINC02293
    nsv4373451copy number variation1nstd173human GRCh37 chr14: 26,562,813-27,424,344 , GRCh38.p12 chr14: 26,093,607-26,955,138 MIR4307, LOC105370418, 8 more genes
    nsv4369325copy number variation1nstd173human GRCh37 chr14: 27,266,981-27,332,381 , GRCh38.p12 chr14: 26,797,775-26,863,175 LINC02294, NOVA1-DT, 1 more genes
    nsv4366765copy number variation1nstd173human GRCh37 chr14: 27,096,267-27,309,098 , GRCh38.p12 chr14: 26,627,061-26,839,892 LINC02293, LINC02294, 1 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
    nsv4225823copy number variation1nstd166human GRCh37.p13 chr14: 27,281,335-27,339,964 , GRCh38.p12 chr14: 26,812,129-26,870,758 LINC02293, LINC02294
    nsv3924892copy number variation1nstd102humanLikely benign GRCh37 chr14: 27,210,934-27,791,995 , NCBI36 chr14: 26,280,774-26,861,835 , GRCh38 chr14: 26,741,728-27,322,789 LOC105370421, MIR3171HG, 9 more genes
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