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Variant : CV801086 (NC_000006.12:g.85556109_85560515del) Homo sapiens

Symbol: CV801086
Name: NC_000006.12:g.85556109_85560515del
Condition: Seizures [RCV001003859]
Clinical Significance: likely pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: SNX14  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: research
HGVS Name(s): NC_000006.12:g.85556109_85560515del
Position
Human AssemblyChrPosition (strand)Source
GRCh37686,265,827 - 86,270,233CLINVAR
Cytogenetic Map66q14.3CLINVAR



Disease Annotations

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 21404938
Created: 2020-03-10
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.