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Variant : CV216079 (GRCh37/hg19 6q26(chr6:162780748-163001030)x1) Homo sapiens

Symbol: CV216079
Name: GRCh37/hg19 6q26(chr6:162780748-163001030)x1
Condition: See cases [RCV000203423]
Clinical Significance: uncertain significance
Last Evaluated: 07/28/2015
Review Status: criteria provided, single submitter
Related Genes: PRKN  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh376162,780,748 - 163,001,030CLINVAR
Cytogenetic Map66q26CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 10766500
Created: 2016-02-09
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.