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Variant : CV227985 (GRCh37/hg19 7q35(chr7:143342375-143913713)) Homo sapiens

Symbol: CV227985
Name: GRCh37/hg19 7q35(chr7:143342375-143913713)
Condition: Abnormality of esophagus morphology [RCV000416661]|Abnormality of the esophagus [RCV000416661]
Clinical Significance: benign
Last Evaluated: 12/15/2015
Review Status: criteria provided, single submitter
Related Genes: ARHGEF35   CTAGE4   CTAGE6   OR2A12   OR2A14   OR2A2   OR2A25   OR2A5   OR2F1   OR2F2   OR6B1   TCAF1   TCAF2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: research
Position
Human AssemblyChrPosition (strand)Source
GRCh377143,342,375 - 143,913,713CLINVAR
Cytogenetic Map77q35CLINVAR
Trait Synonyms: Anomaly of the esophagus



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12791369
Created: 2017-03-07
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.