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Variant : CV535559 (NC_000003.12:g.(?_196154147)_(197376501_?)del) Homo sapiens

Symbol: CV535559
Name: NC_000003.12:g.(?_196154147)_(197376501_?)del
Condition: Schizophrenia [RCV000754279]
Clinical Significance: pathogenic
Last Evaluated: 03/20/2018
Review Status: criteria provided, single submitter
Related Genes: CEP19   DLG1   DLG1-AS1   FBXO45   LINC00885   LINC01063   MELTF   MELTF-AS1   MIR4797   NCBP2   NCBP2-AS1   NCBP2AS2   NRROS   PAK2   PCYT1A   PIGX   PIGZ   RNF168   SENP5   SLC51A   SMCO1   TCTEX1D2   TM4SF19   TM4SF19-AS1   TM4SF19-TCTEX1D2   UBXN7   UBXN7-AS1   WDR53   ZDHHC19  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: research
HGVS Name(s): NC_000003.12:g.(?_196154147)_(197376501_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh383196,154,147 - 197,376,501CLINVAR
Cytogenetic Map33q29CLINVAR
Trait Synonyms: SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14352316
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-08-04
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.