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Variant : CV554434 (GRCh37/hg19 6q26(chr6:162545871-163112949)x3) Homo sapiens

Symbol: CV554434
Name: GRCh37/hg19 6q26(chr6:162545871-163112949)x3
Condition: not provided [RCV000682739]
Clinical Significance: uncertain significance
Last Evaluated: 11/28/2017
Review Status: no assertion criteria provided
Related Genes: PRKN  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh376162,545,871 - 163,112,949CLINVAR
Cytogenetic Map66q26CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13795639
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-11-12
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.