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Variant : CV550812 (Single allele) Homo sapiens

Symbol: CV550812
Name: Single allele
Condition: not provided [RCV000677973]
Clinical Significance: uncertain significance
Last Evaluated: 10/30/2017
Review Status: criteria provided, single submitter
Related Genes: CACNG2   EIF3D   FOXRED2   TXN2  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: provider interpretation
Position
Human AssemblyChrPosition (strand)Source
GRCh372236,785,240 - 36,995,848CLINVAR
Cytogenetic Map2222q12.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13790611
Created: 2018-09-11
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.