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Items: 1 to 20 of 414

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5977724copy number variation2nstd209human GRCh38 chrX: 3,821,679-3,826,516 , GRCh37.p13 chrX: 3,739,720-3,744,557 LOC389906
    nsv5975968copy number variation2nstd209human GRCh38 chrX: 3,814,155-3,822,064 , GRCh37.p13 chrX: 3,732,196-3,740,105 LOC389906
    nsv5975923copy number variation2nstd209human GRCh38 chrX: 3,821,079-3,825,866 , GRCh37.p13 chrX: 3,739,120-3,743,907 LOC389906
    nsv5972086copy number variation2nstd209human GRCh38 chrX: 3,815,363-3,824,731 , GRCh37.p13 chrX: 3,733,404-3,742,772 LOC389906
    nsv5971641copy number variation1nstd209human GRCh38 chrX: 3,814,154-3,816,224 , GRCh37.p13 chrX: 3,732,195-3,734,265 LOC389906
    nsv5971411copy number variation2nstd209human GRCh38 chrX: 3,823,574-3,829,779 , GRCh37.p13 chrX: 3,741,615-3,747,820 LOC389906
    nsv5968688copy number variation2nstd209human GRCh38 chrX: 3,823,795-3,828,023 , GRCh37.p13 chrX: 3,741,836-3,746,064 LOC389906
    nsv5870259copy number variation1nstd209human GRCh38 chrX: 3,814,191-3,826,285 , GRCh37.p13 chrX: 3,732,232-3,744,326 LOC389906
    nsv5670630copy number variation1nstd207human GRCh38 chrX: 3,823,830-3,900,671 , GRCh37.p13 chrX: 3,741,871-3,818,712 LOC389906, FAM239B, 3 more genes
    nsv5667767copy number variation1nstd207human GRCh38 chrX: 3,818,460-3,818,522 , GRCh37.p13 chrX: 3,736,501-3,736,563 LOC389906
    nsv5667165copy number variation1nstd207human GRCh38 chrX: 3,821,478-3,823,068 , GRCh37.p13 chrX: 3,739,519-3,741,109 LOC389906
    nsv5667014copy number variation1nstd207human GRCh38 chrX: 3,821,116-3,821,262 , GRCh37.p13 chrX: 3,739,157-3,739,303 LOC389906
    nsv5666696copy number variation1nstd207human GRCh38 chrX: 3,818,622-3,823,306 , GRCh37.p13 chrX: 3,736,663-3,741,347 LOC389906
    nsv5666520copy number variation1nstd207human GRCh38 chrX: 3,823,169-3,861,584 , GRCh37.p13 chrX: 3,741,210-3,779,625 LOC389906, TRI-GAT1-1, 1 more genes
    nsv5422978copy number variation1nstd206human GRCh38 chrX: 3,677,752-4,945,864 , GRCh37.p13 chrX: 3,595,793-4,863,905 PRKX, LOC101928201, 9 more genes
    nsv5421782copy number variation1nstd206human GRCh38 chrX: 3,817,000-3,831,450 , GRCh37.p13 chrX: 3,735,041-3,749,491 LOC389906
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4893678copy number variation1nstd200human GRCh38 chrX: 3,814,242-3,826,258 , GRCh37.p13 chrX: 3,732,283-3,744,299 LOC389906
    nsv4769315copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-4,857,212 , GRCh38.p12 chrX: 10,001-4,939,171 AKAP17A, RPS27AP20, 58 more genes
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