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Variant : CV593165 (GRCh37/hg19 14q21.1(chr14:39632114-39633213)x1) Homo sapiens

Symbol: CV593165
Name: GRCh37/hg19 14q21.1(chr14:39632114-39633213)x1
Condition: not provided [RCV000738465]
Clinical Significance: benign
Last Evaluated: 05/23/2001
Review Status: no assertion criteria provided
Related Genes: TRAPPC6B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371439,632,114 - 39,633,213CLINVAR
Cytogenetic Map1414q21.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14353845
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-20
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.