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Variant : CV225943 (NC_000006.12:g.(?_162146194)_(162225195_?)del) Homo sapiens

Symbol: CV225943
Name: NC_000006.12:g.(?_162146194)_(162225195_?)del
Condition: Schizophrenia [RCV000416903]
Clinical Significance: likely pathogenic
Last Evaluated: 02/19/2016
Review Status: criteria provided, single submitter
Related Genes: PRKN  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: research
HGVS Name(s): NC_000006.12:g.(?_162146194)_(162225195_?)del
NC_000006.10:g.(?_162487216)_(162566217_?)del
NC_000006.11:g.(?_162567226)_(162646227_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh386162,146,194 - 162,225,195CLINVAR
GRCh376162,567,226 - 162,646,227CLINVAR
Build 366162,487,216 - 162,566,217CLINVAR
Cytogenetic Map66q26CLINVAR
Trait Synonyms: SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER




Additional Information

 
CRRD Object Information
CRRD ID: 12791640
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.