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Variant : CV535537 (NC_000022.11:g.(?_22638171)_(23320336_?)del) Homo sapiens

Symbol: CV535537
Name: NC_000022.11:g.(?_22638171)_(23320336_?)del
Condition: Schizophrenia [RCV000754257]
Clinical Significance: likely pathogenic
Last Evaluated: 03/20/2018
Review Status: criteria provided, single submitter
Related Genes: BCR   GGTLC2   GNAZ   IGL   IGLC1   IGLC2   IGLC3   IGLC7   IGLJ1   IGLJ2   IGLJ3   IGLJ4   IGLJ5   IGLJ6   IGLJ7   IGLL5   IGLV2-11   IGLV2-14   IGLV2-18   IGLV2-23   IGLV2-8   IGLV3-1   IGLV3-10   IGLV3-12   IGLV3-16   IGLV3-19   IGLV3-21   IGLV3-22   IGLV3-25   IGLV3-27   IGLV3-9   IGLV4-3   MIR5571   MIR650   RAB36   RSPH14  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: research
HGVS Name(s): NC_000022.11:g.(?_22638171)_(23320336_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh382222,638,171 - 23,320,336CLINVAR
Cytogenetic Map2222q11.22-11.23CLINVAR
Trait Synonyms: SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14351906
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-09-08
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.