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Variant : CV535467 (NC_000016.10:g.(?_29627836)_(30184960_?)del) Homo sapiens

Symbol: CV535467
Name: NC_000016.10:g.(?_29627836)_(30184960_?)del
Condition: Schizophrenia [RCV000754187]
Clinical Significance: pathogenic
Last Evaluated: 03/20/2018
Review Status: criteria provided, single submitter
Related Genes: ALDOA   ALDOA   ASPHD1   C16orf54   C16orf92   CDIPT   CDIPTOSP   CORO1A   DOC2A   GDPD3   HIRIP3   INO80E   KCTD13   KIF22   MAPK3   MAZ   MVP   PAGR1   PPP4C   PRRT2   QPRT   SEZ6L2   SPN   TAOK2   TBX6   TLCD3B   TMEM219   YPEL3   ZG16  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: research
HGVS Name(s): NC_000016.10:g.(?_29627836)_(30184960_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381629,627,836 - 30,184,960CLINVAR
Cytogenetic Map1616p11.2CLINVAR
Trait Synonyms: SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14352220
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.