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Variant : CV599882 (GRCh37/hg19 5q31.1(chr5:134258183-134263961)x3) Homo sapiens

Symbol: CV599882
Name: GRCh37/hg19 5q31.1(chr5:134258183-134263961)x3
Condition: not provided [RCV000745182]
Clinical Significance: benign
Last Evaluated: 04/10/2012
Review Status: no assertion criteria provided
Related Genes: PCBD2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh375134,258,183 - 134,263,961CLINVAR
Cytogenetic Map55q31.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14360550
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-11
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.