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Variant : CV225937 (NC_000003.12:g.(?_196011149)_(197606127_?)del) Homo sapiens

Symbol: CV225937
Name: NC_000003.12:g.(?_196011149)_(197606127_?)del
Condition: Schizophrenia [RCV000416880]
Clinical Significance: pathogenic
Last Evaluated: 02/19/2016
Review Status: criteria provided, single submitter
Related Genes: BDH1   CEP19   DLG1   DLG1-AS1   FBXO45   LINC00885   LINC01063   LINC02012   MELTF   MELTF-AS1   MIR4797   NCBP2   NCBP2AS2   NRROS   PAK2   PCYT1A   PIGX   PIGZ   RNF168   SENP5   SLC51A   SMCO1   TCTEX1D2   TFRC   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.(?_196011149)_(197606127_?)del
NC_000003.10:g.(?_197222417)_(198817395_?)del
NC_000003.11:g.(?_195738020)_(197332998_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh383196,011,149 - 197,606,127CLINVAR
GRCh373195,738,020 - 197,332,998CLINVAR
Build 363197,222,417 - 198,817,395CLINVAR
Cytogenetic Map33q29CLINVAR
Trait Synonyms: SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER




Additional Information

 
CRRD Object Information
CRRD ID: 12791627
Created: 2017-03-07
Species: Homo sapiens
Last Modified: 2018-01-30
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.