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Variant : CV437362 (GRCh37/hg19 6q26(chr6:162638345-162754162)x0) Homo sapiens

Symbol: CV437362
Name: GRCh37/hg19 6q26(chr6:162638345-162754162)x0
Condition: See cases [RCV000510284]
Clinical Significance: pathogenic
Last Evaluated: 09/01/2015
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
GRCh376162,638,345 - 162,754,162CLINVAR
Cytogenetic Map66q26CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443264
Created: 2017-11-07
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.