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Variant : CV436869 (GRCh37/hg19 6q26(chr6:162754605-163163098)x1) Homo sapiens

Symbol: CV436869
Name: GRCh37/hg19 6q26(chr6:162754605-163163098)x1
Condition: See cases [RCV000512111]
Clinical Significance: uncertain significance
Last Evaluated: 07/01/2014
Review Status: no assertion criteria provided
Related Genes: PACRG   PRKN  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh376162,754,605 - 163,163,098CLINVAR
Cytogenetic Map66q26CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13445079
Created: 2017-11-07
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.