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Items: 1 to 20 of 447

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6117300copy number variation1nstd186human GRCh37 chrX: 105,110,257-105,110,464 , GRCh38.p12 chrX: 105,866,264-105,866,471 NRK
    nsv6117035copy number variation1nstd186human GRCh37 chrX: 105,191,172-105,191,459 , GRCh38.p12 chrX: 105,947,180-105,947,467 NRK
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5884236copy number variation1nstd209human GRCh38 chrX: 105,866,261-105,866,470 , GRCh37.p13 chrX: 105,110,254-105,110,463 NRK
    nsv5874346copy number variation1nstd209human GRCh38 chrX: 105,826,224-105,826,283 , GRCh37.p13 chrX: 105,070,217-105,070,276 NRK
    nsv5869468copy number variation1nstd209human GRCh38 chrX: 105,947,164-105,947,466 , GRCh37.p13 chrX: 105,191,156-105,191,458 NRK
    nsv5867845copy number variation1nstd209human GRCh38 chrX: 105,918,099-105,918,334 , GRCh37.p13 chrX: 105,162,091-105,162,326 NRK
    nsv5728541mobile element insertion1nstd211human GRCh38 chrX: 105,921,869-105,921,869 , GRCh37.p13 chrX: 105,165,861-105,165,861 NRK
    nsv5725326mobile element insertion1nstd211human GRCh38 chrX: 105,922,809-105,922,809 , GRCh37.p13 chrX: 105,166,801-105,166,801 NRK
    nsv5719218mobile element insertion1nstd211human GRCh38 chrX: 105,869,623-105,869,623 , GRCh37.p13 chrX: 105,113,616-105,113,616 NRK
    nsv5667006copy number variation1nstd207human GRCh38 chrX: 105,826,224-105,826,283 , GRCh37.p13 chrX: 105,070,217-105,070,276 NRK
    nsv5665028copy number variation1nstd207human GRCh38 chrX: 105,947,164-105,947,466 , GRCh37.p13 chrX: 105,191,156-105,191,458 NRK
    nsv5555756mobile element insertion1nstd206human GRCh38 chrX: 105,869,623-105,869,674 , GRCh37.p13 chrX: 105,113,616-105,113,667 NRK
    nsv5433078copy number variation1nstd206human GRCh38 chrX: 105,887,097-105,888,489 , GRCh37.p13 chrX: 105,131,090-105,132,482 NRK
    nsv5428475copy number variation1nstd206human GRCh38 chrX: 105,826,198-105,826,310 , GRCh37.p13 chrX: 105,070,191-105,070,303 NRK
    nsv5428324copy number variation1nstd206human GRCh38 chrX: 105,866,264-105,866,471 , GRCh37.p13 chrX: 105,110,257-105,110,464 NRK
    nsv5427345copy number variation1nstd206human GRCh38 chrX: 105,826,249-105,826,307 , GRCh37.p13 chrX: 105,070,242-105,070,300 NRK
    nsv5420327copy number variation1nstd206human GRCh38 chrX: 105,958,613-105,959,695 , GRCh37.p13 chrX: 105,202,605-105,203,687 LOC105373304, NRK
    nsv5418001copy number variation1nstd206human GRCh38 chrX: 105,872,113-105,874,115 , GRCh37.p13 chrX: 105,116,106-105,118,108 NRK
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