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Variant : CV651583 (NC_000006.11:g.(?_162622143)_(163148721_?)dup) Homo sapiens

Symbol: CV651583
Name: NC_000006.11:g.(?_162622143)_(163148721_?)dup
Condition: Parkinson disease 2 [RCV000820597]
Clinical Significance: uncertain significance
Last Evaluated: 08/14/2018
Review Status: criteria provided, single submitter
Related Genes: PACRG   PRKN  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000006.11:g.(?_162622143)_(163148721_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh386162,201,111 - 162,727,689CLINVAR
GRCh376162,622,143 - 163,148,721CLINVAR
Cytogenetic Map66q26CLINVAR
Trait Synonyms: Parkin Type of Early-Onset Parkinson Disease; Parkin Type of Juvenile Parkinson Disease



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14701961
Created: 2019-09-06
Species: Homo sapiens
Last Modified: 2019-12-03
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.