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Items: 1 to 20 of 521

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949931insertion1nstd209human GRCh38 chr5: 16,098,767-16,098,767 , GRCh37.p13 chr5: 16,098,876-16,098,876 MARCHF11
    nsv5905306copy number variation1nstd209human GRCh38 chr5: 16,124,701-16,125,376 , GRCh37.p13 chr5: 16,124,810-16,125,485 MARCHF11, MARCHF11-AS1
    nsv5904616copy number variation1nstd209human GRCh38 chr5: 16,093,033-16,093,090 , GRCh37.p13 chr5: 16,093,142-16,093,199 MARCHF11
    nsv5899559copy number variation1nstd209human GRCh38 chr5: 16,103,888-16,103,939 , GRCh37.p13 chr5: 16,103,997-16,104,048 MARCHF11
    nsv5888941copy number variation1nstd209human GRCh38 chr5: 16,149,903-16,150,669 , GRCh37.p13 chr5: 16,150,012-16,150,778 MARCHF11
    nsv5841520copy number variation1nstd209human GRCh38 chr5: 16,128,744-16,130,073 , GRCh37.p13 chr5: 16,128,853-16,130,182 MARCHF11-AS1, MARCHF11
    nsv5723926mobile element insertion2nstd211human GRCh38 chr5: 16,066,155-16,066,155 , GRCh37.p13 chr5: 16,066,264-16,066,264 MARCHF11
    nsv5719522mobile element insertion2nstd211human GRCh38 chr5: 16,098,779-16,098,779 , GRCh37.p13 chr5: 16,098,888-16,098,888 MARCHF11
    nsv5636311insertion1nstd207human GRCh38 chr5: 16,166,956-16,166,956 , GRCh37.p13 chr5: 16,167,065-16,167,065 MARCHF11
    nsv5626547insertion1nstd207human GRCh38 chr5: 16,098,767-16,098,767 , GRCh37.p13 chr5: 16,098,876-16,098,876 MARCHF11
    nsv5571898copy number variation1nstd207human GRCh38 chr5: 16,124,703-16,125,379 , GRCh37.p13 chr5: 16,124,812-16,125,488 MARCHF11-AS1, MARCHF11
    nsv5566076copy number variation1nstd207human GRCh38 chr5: 16,149,903-16,150,669 , GRCh37.p13 chr5: 16,150,012-16,150,778 MARCHF11
    nsv5555627mobile element insertion1nstd206human GRCh38 chr5: 16,066,155-16,066,206 , GRCh37.p13 chr5: 16,066,264-16,066,315 MARCHF11
    nsv5536107insertion1nstd206human GRCh38 chr5: 16,098,767-16,098,767 , GRCh37.p13 chr5: 16,098,876-16,098,876 MARCHF11
    nsv5473631copy number variation1nstd206human GRCh38 chr5: 16,100,953-16,103,921 , GRCh37.p13 chr5: 16,101,062-16,104,030 MARCHF11
    nsv5470032copy number variation1nstd206human GRCh38 chr5: 16,124,701-16,125,382 , GRCh37.p13 chr5: 16,124,810-16,125,491 MARCHF11, MARCHF11-AS1
    nsv5462570copy number variation1nstd206human GRCh38 chr5: 16,170,638-16,170,707 , GRCh37.p13 chr5: 16,170,747-16,170,816 MARCHF11
    nsv5462548copy number variation1nstd206human GRCh38 chr5: 16,149,906-16,150,670 , GRCh37.p13 chr5: 16,150,015-16,150,779 MARCHF11
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv5328396translocation1nstd204human GRCh38.p13 chr5: 16,150,670-16,150,670 , GRCh38.p13 chr5: 16,149,906-16,149,906 , GRCh37.p13 chr5: 16,150,015-16,150,015 , GRCh37.p13 chr5: 16,150,779-16,150,779 MARCHF11
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