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Variant : CV381691 (GRCh37/hg19 6q26(chr6:163000261-163089344)x1) Homo sapiens

Symbol: CV381691
Name: GRCh37/hg19 6q26(chr6:163000261-163089344)x1
Condition: See cases [RCV000446737]
Clinical Significance: benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: PRKN  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh376163,000,261 - 163,089,344CLINVAR
Cytogenetic Map66q26CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12851460
Created: 2017-04-11
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.