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Variant : CV535644 (Single allele) Homo sapiens

Symbol: CV535644
Name: Single allele
Condition: Schizophrenia [RCV000754364]
Clinical Significance: likely pathogenic
Last Evaluated: 03/20/2018
Review Status: criteria provided, single submitter
Related Genes: ALG13   AMMECR1   AMOT   CAPN6   CHRDL1   DCX   HTR2C   IL13RA2   LHFPL1   LRCH2   MIR1264   MIR1298   MIR1911   MIR1912   MIR3978   MIR4329   MIR448   MIR764   PAK3   RBMXL3   RTL4   RTL9   SERTM2   SNORA35   SNORA35B   SNORD96B   TMEM164   TRPC5   TRPC5OS   XACT  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: research
Position
Human AssemblyChrPosition (strand)Source
GRCh38X110,074,915 - 115,196,481CLINVAR
Cytogenetic MapXXq23CLINVAR
Trait Synonyms: SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14350993
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-10-15
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.