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Variant : CV818836 (NC_000001.11:g.(?_11012634)_(11934865_?)del) Homo sapiens

Symbol: CV818836
Name: NC_000001.11:g.(?_11012634)_(11934865_?)del
Condition: Atrial fibrillation, familial, 6 [RCV001031444]
Clinical Significance: uncertain significance
Last Evaluated: 08/01/2019
Review Status: criteria provided, single submitter
Related Genes: AGTRAP   ANGPTL7   C1orf167   CLCN6   DISP3   DRAXIN   EXOSC10   FBXO2   FBXO44   FBXO6   KIAA2013   MAD2L2   MASP2   MTHFR   MTOR   NPPA   NPPB   PLOD1   SRM   TARDBP   UBIAD1  
Variant Type: deletion (SO:0000159)
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_11012634)_(11934865_?)del
Human AssemblyChrPosition (strand)Source
GRCh37111,072,691 - 11,994,922CLINVAR
Cytogenetic Map11p36.22CLINVAR

Disease Annotations
References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 26889905
Created: 2020-05-12
Species: Homo sapiens
Last Modified: 2020-10-15
Status: ACTIVE


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