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Variant : CV262759 (Single allele) Homo sapiens

Symbol: CV262759
Name: Single allele
Condition: 16q24.3 microdeletion syndrome [RCV000258201]
Clinical Significance: pathogenic
Last Evaluated: 08/01/2016
Review Status: no assertion criteria provided
Related Genes: ACSF3   ANKRD11   APRT   CBFA2T3   CDH15   CDT1   CTU2   CYBA   GALNS   IL17C   MVD   PABPN1L   PIEZO1   RNF166   SLC22A31   SNAI3   TRAPPC2L   ZC3H18   ZNF778  
Variant Type: deletion (SO:0000159)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371688,666,177 - 89,472,627CLINVAR
Cytogenetic Map1616q24.2-24.3CLINVAR

Disease Annotations

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 11567281
Created: 2016-12-06
Species: Homo sapiens
Last Modified: 2020-10-20
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.