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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957793copy number variation1nstd209human GRCh38 chr22: 41,232,160-41,458,145 , GRCh37.p13 chr22: 41,628,164-41,854,149 ZC3H7B, LOC105373042, 9 more genes
    nsv5956471copy number variation1nstd209human GRCh38 chr22: 41,456,449-41,458,051 , GRCh37.p13 chr22: 41,852,453-41,854,055 PHF5A
    nsv5874441copy number variation2nstd209human GRCh38 chr22: 41,456,341-41,458,040 , GRCh37.p13 chr22: 41,852,345-41,854,044 PHF5A
    nsv5299062copy number variation1nstd204human GRCh38.p13 chr22: 41,442,501-41,665,900 , GRCh37.p13 chr22: 41,838,505-42,061,904 CSDC2, LOC105373043, 8 more genes
    nsv5293624copy number variation1nstd204human GRCh38.p13 chr22: 41,236,101-41,543,100 , GRCh37.p13 chr22: 41,632,105-41,939,104 LOC105373042, RANGAP1, 11 more genes
    nsv5286543copy number variation1nstd204human GRCh38.p13 chr22: 41,468,768-41,471,367 , GRCh37.p13 chr22: 41,864,772-41,867,371 PHF5A, ACO2
    nsv5281292copy number variation1nstd204human GRCh38.p13 chr22: 41,124,301-41,900,100 , GRCh37.p13 chr22: 41,520,305-42,296,104 SNU13, RANGAP1, 34 more genes
    nsv5038075copy number variation1nstd200human GRCh38 chr22: 41,456,906-41,458,109 , GRCh37.p13 chr22: 41,852,910-41,854,113 PHF5A
    nsv5032425inversion1nstd200human GRCh38 chr22: 41,452,969-44,153,937 , GRCh37.p13 chr22: 41,848,973-44,549,817 , LOC101927393, 95 more genes
    nsv5029647copy number variation1nstd200human GRCh38 chr22: 41,456,477-41,458,081 , GRCh37.p13 chr22: 41,852,481-41,854,085 PHF5A
    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
    nsv4729846copy number variation1nstd102humanUncertain significance GRCh37 chr22: 41,853,620-42,385,978 , GRCh38.p12 chr22: 41,457,616-41,989,974 RNU6ATAC22P, CSDC2, 23 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
    nsv4676232copy number variation1nstd102humanPathogenic GRCh37 chr22: 40,502,364-51,197,838 , GRCh38.p12 chr22: 40,106,360-50,759,410 MIR378I, SNORD13P1, 274 more genes
    nsv4536948copy number variation1nstd166human GRCh37.p13 chr22: 41,853,954-41,854,052 , GRCh38.p12 chr22: 41,457,950-41,458,048 PHF5A
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4457420copy number variation2nstd102humannot provided, Uncertain significance GRCh37 chr22: 41,742,988-41,946,225 , GRCh38.p12 chr22: 41,346,984-41,550,221 LOC105373042, TEF, 9 more genes
    nsv4284762copy number variation1nstd166human GRCh37.p13 chr22: 41,862,500-41,868,000 , GRCh38.p12 chr22: 41,466,496-41,471,996 ACO2, PHF5A
    nsv3924136copy number variation1nstd102humanPathogenic GRCh38 chr22: 40,202,014-50,735,806 , GRCh37 chr22: 40,598,018-51,174,234 , NCBI36 chr22: 38,927,964-49,521,100 CYP2D8P, TBC1D22A-AS1, 270 more genes
    nsv3919881copy number variation1nstd102humanPathogenic GRCh37 chr22: 17,397,633-51,178,213 , GRCh38 chr22: 16,916,743-50,739,785 , NCBI36 chr22: 15,777,633-49,525,079 MIR12114, MIR6820, 1059 more genes
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