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Variant : CV535520 (NC_000022.11:g.(?_18159879)_(21362822_?)del) Homo sapiens

Symbol: CV535520
Name: NC_000022.11:g.(?_18159879)_(21362822_?)del
Condition: Schizophrenia [RCV000754240]
Clinical Significance: pathogenic
Last Evaluated: 03/20/2018
Review Status: criteria provided, single submitter
Related Genes: AIFM3   ARVCF   C22orf39   CCDC188   CDC45   CLDN5   CLTCL1   COMT   CRKL   DGCR11   DGCR2   DGCR5   DGCR6   DGCR6L   DGCR8   ESS2   FAM230A   FAM230B   FAM230D   FAM230E   FAM230F   FAM230G   FAM230H   FAM230J   GGT2   GGTLC3   GNB1L   GP1BB   GSC2   HIRA   HSERVPRODH   KLHL22   LINC00895   LINC00896   LINC01311   LINC01637   LINC01651   LINC02891   LOC108510655   LOC110120888   LOC110121413   LOC112694764   LOC112694766   LOC112694767   LOC114004361   LOC116309126   LOC116309127   LRRC74B   LZTR1   MED15   MIR1286   MIR1306   MIR185   MIR3618   MIR4761   MIR649   MIR6816   MRPL40   P2RX6   PI4KA   PRODH   RANBP1   RIMBP3   RTL10   RTN4R   SCARF2   SEPTIN5   SEPTIN5   SERPIND1   SLC25A1   SLC7A4   SNAP29   SNORA77B   TANGO2   TBX1   THAP7   THAP7-AS1   TMEM191B   TRMT2A   TSSK2   TXNRD2   UFD1   USP18   USP41   ZDHHC8   ZNF74  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: research
HGVS Name(s): NC_000022.11:g.(?_18159879)_(21362822_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh382218,159,879 - 21,362,822CLINVAR
Cytogenetic Map2222q11.21CLINVAR
Trait Synonyms: SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14351831
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-11-17
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.