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Variant : CV595922 (GRCh37/hg19 20q13.12(chr20:42264653-42275499)x0) Homo sapiens

Symbol: CV595922
Name: GRCh37/hg19 20q13.12(chr20:42264653-42275499)x0
Condition: not provided [RCV000741222]
Clinical Significance: benign
Last Evaluated: 06/01/2011
Review Status: no assertion criteria provided
Related Genes: IFT52  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372042,264,653 - 42,275,499CLINVAR
Cytogenetic Map2020q13.12CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14356596
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-14
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.