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Variant : CV437342 (GRCh37/hg19 2p16.1(chr2:55588867-56927117)x1) Homo sapiens

Symbol: CV437342
Name: GRCh37/hg19 2p16.1(chr2:55588867-56927117)x1
Condition: See cases [RCV000510380]
Clinical Significance: uncertain significance
Last Evaluated: 05/22/2013
Review Status: no assertion criteria provided
Related Genes: CCDC85A   CCDC88A   CFAP36   EFEMP1   MIR216A   MIR217   PNPT1   PPP4R3B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37255,588,867 - 56,927,117CLINVAR
Cytogenetic Map22p16.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13443359
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-03-24
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.