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Variant : CV226029 (NC_000022.10:g.(?_23667751)_(24991609_?)dup) Homo sapiens

Symbol: CV226029
Name: NC_000022.10:g.(?_23667751)_(24991609_?)dup
Condition: Schizophrenia [RCV000416915]
Clinical Significance: likely pathogenic
Last Evaluated: 02/19/2016
Review Status: criteria provided, single submitter
Related Genes: ADORA2A   C22orf15   CABIN1   CHCHD10   DDT   DDTL   DERL3   DRICH1   GGT1   GGT5   GSTT1   GSTT2   GSTT2B   GUCD1   IGLL1   LRRC75B   MIF   MMP11   RGL4   SLC2A11   SMARCB1   SNRPD3   SPECC1L   SUSD2   UPB1   VPREB3   ZNF70  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: research
HGVS Name(s): NC_000022.10:g.(?_23667751)_(24991609_?)dup
NC_000022.9:g.(?_21997751)_(23321609_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh372223,667,751 - 24,991,609CLINVAR
Build 362221,997,751 - 23,321,609CLINVAR
Cytogenetic Map2222q11.23CLINVAR
Trait Synonyms: SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER




Additional Information

 
RGD Object Information
RGD ID: 12791644
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.