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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960300copy number variation1nstd209human GRCh38 chr22: 39,029,440-39,049,501 , GRCh37.p13 chr22: 39,425,445-39,445,506 APOBEC3D, APOBEC3F
    nsv5885734copy number variation1nstd209human GRCh38 chr22: 39,030,398-39,037,437 , GRCh37.p13 chr22: 39,426,403-39,433,442 APOBEC3F, APOBEC3D
    nsv5551582copy number variation1nstd206human GRCh38 chr22: 39,030,132-39,050,500 , GRCh37.p13 chr22: 39,426,137-39,446,505 APOBEC3D, APOBEC3F
    nsv5546920copy number variation1nstd206human GRCh38 chr22: 39,031,269-39,048,555 , GRCh37.p13 chr22: 39,427,274-39,444,560 APOBEC3D, APOBEC3F
    nsv5544193copy number variation1nstd206human GRCh38 chr22: 38,997,239-39,050,425 , GRCh37.p13 chr22: 39,393,244-39,446,430 APOBEC3F, APOBEC3B-AS1, 2 more genes
    nsv5323513copy number variation1nstd204human GRCh37.p13 chr22: 39,426,564-39,446,780 , GRCh38.p13 chr22: 39,030,559-39,050,775 APOBEC3F, APOBEC3D
    nsv5298512copy number variation1nstd204human GRCh38.p13 chr22: 39,029,586-39,050,597 , GRCh37.p13 chr22: 39,425,591-39,446,602 APOBEC3F, APOBEC3D
    nsv5288097copy number variation1nstd204human GRCh38.p13 chr22: 38,982,101-39,534,900 , GRCh37.p13 chr22: 39,378,106-39,930,905 APOBEC3C, COX5BP7, 25 more genes
    nsv5283206copy number variation1nstd204human GRCh38.p13 chr22: 39,029,601-39,049,900 , GRCh37.p13 chr22: 39,425,606-39,445,905 APOBEC3D, APOBEC3F
    nsv5282051copy number variation1nstd204human GRCh38.p13 chr22: 39,031,305-39,032,376 , GRCh37.p13 chr22: 39,427,310-39,428,381 APOBEC3F, APOBEC3D
    nsv5038088copy number variation1nstd200human GRCh38 chr22: 39,031,269-39,048,555 , GRCh37.p13 chr22: 39,427,274-39,444,560 APOBEC3F, APOBEC3D
    nsv5036315copy number variation1nstd200human GRCh38 chr22: 39,032,640-39,037,244 , GRCh37.p13 chr22: 39,428,645-39,433,249 APOBEC3D, APOBEC3F
    nsv5034620copy number variation1nstd200human GRCh38 chr22: 39,030,540-39,050,782 , GRCh37.p13 chr22: 39,426,545-39,446,787 APOBEC3D, APOBEC3F
    nsv5032395copy number variation1nstd200human GRCh38 chr22: 39,032,779-39,038,881 , GRCh37.p13 chr22: 39,428,784-39,434,886 APOBEC3D, APOBEC3F
    nsv4885669copy number variation1nstd200human GRCh37 chr22: 39,426,573-39,446,773 , GRCh38.p12 chr22: 39,030,568-39,050,768 APOBEC3F, APOBEC3D
    nsv4882800copy number variation1nstd200human GRCh37 chr22: 39,427,274-39,444,560 , GRCh38.p12 chr22: 39,031,269-39,048,555 APOBEC3D, APOBEC3F
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4669747copy number variation1nstd186human GRCh37 chr22: 39,426,703-39,443,920 , GRCh38.p12 chr22: 39,030,698-39,047,915 APOBEC3D, APOBEC3F
    nsv4629430copy number variation2nstd183human GRCh37 chr22: 39,426,703-39,443,920 , GRCh38.p12 chr22: 39,030,698-39,047,915 APOBEC3D, APOBEC3F
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