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Items: 1 to 20 of 124

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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
    nsv5881657copy number variation1nstd209human GRCh38 chr22: 41,232,219-41,269,154 , GRCh37.p13 chr22: 41,628,223-41,665,158 RANGAP1, CHADL, 1 more genes
    nsv5870551copy number variation1nstd209human GRCh38 chr22: 41,234,630-41,237,029 , GRCh37.p13 chr22: 41,630,634-41,633,033 CHADL
    nsv5551836copy number variation1nstd206human GRCh38 chr22: 41,232,031-41,233,299 , GRCh37.p13 chr22: 41,628,035-41,629,303 CHADL
    nsv5543106copy number variation1nstd206human GRCh38 chr22: 41,241,788-41,243,763 , GRCh37.p13 chr22: 41,637,792-41,639,767 RANGAP1, CHADL
    nsv5375711translocation1nstd200human GRCh38 chr22: 41,232,097-41,232,097 , GRCh38 chr22: 41,233,181-41,233,181 , GRCh37.p13 chr22: 41,629,185-41,629,185 , GRCh37.p13 chr22: 41,628,101-41,628,101 CHADL
    nsv5320976copy number variation1nstd204human GRCh38.p13 chr22: 41,232,165-41,233,255 , GRCh37.p13 chr22: 41,628,169-41,629,259 CHADL
    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
    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
    nsv5036337copy number variation1nstd200human GRCh38 chr22: 41,232,008-41,271,618 , GRCh37.p13 chr22: 41,628,012-41,667,622 MIR6889, RANGAP1, 1 more genes
    nsv5035721copy number variation1nstd200human GRCh38 chr22: 41,183,197-41,231,815 , GRCh37.p13 chr22: 41,579,201-41,627,819 LOC646927, L3MBTL2-AS1, 4 more genes
    nsv5035709copy number variation1nstd200human GRCh38 chr22: 41,241,834-41,243,694 , GRCh37.p13 chr22: 41,637,838-41,639,698 RANGAP1, CHADL
    nsv5034861copy number variation1nstd200human GRCh38 chr22: 41,240,926-41,244,788 , GRCh37.p13 chr22: 41,636,930-41,640,792 CHADL, RANGAP1
    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
    nsv4707411copy number variation1nstd195human GRCh37 chr22: 41,637,832-41,637,833 , GRCh38.p12 chr22: 41,241,828-41,241,829 CHADL
    nsv4680014copy number variation1nstd189human GRCh37.p13 chr22: 40,744,858-41,816,746 , GRCh38.p12 chr22: 40,348,854-41,420,742 , ADSL, 37 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
    nsv4672358copy number variation1nstd186human GRCh37 chr22: 41,637,832-41,639,747 , GRCh38.p12 chr22: 41,241,828-41,243,743 CHADL, RANGAP1
    nsv4623738copy number variation1nstd183human GRCh37 chr22: 41,637,832-41,639,747 , GRCh38.p12 chr22: 41,241,828-41,243,743 RANGAP1, CHADL
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