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Variant : CV167185 (Single allele) Homo sapiens

Symbol: CV167185
Name: Single allele
Condition: Normal pregnancy [RCV000161751]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: IGH   IGHA1   IGHA2   IGHD   IGHD3-3   IGHE   IGHG1   IGHG2   IGHG3   IGHG4   IGHM   IGHV3-23  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: case-control
Position
Human AssemblyChrPosition (strand)Source
GRCh3714105,998,544 - 107,287,663CLINVAR
Cytogenetic Map1414q32.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9832160
Created: 2015-03-10
Species: Homo sapiens
Last Modified: 2020-07-28
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.