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Variant : CV158605 (GRCh38/hg38 10q23.33-24.1(chr10:92643919-95471137)x1) Homo sapiens

Symbol: CV158605
Name: GRCh38/hg38 10q23.33-24.1(chr10:92643919-95471137)x1
Condition: See cases [RCV000137919]
Clinical Significance: pathogenic
Last Evaluated: 11/04/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ACSM6   CEP55   CYP26A1   CYP26C1   CYP2C18   CYP2C19   CYP2C8   CYP2C9   EXOC6   FFAR4   FRA10AC1   HELLS   HHEX   KIF11   LGI1   MYOF   NOC3L   PDE6C   PDLIM1   PLCE1   PLCE1-AS1   PLCE1-AS2   RBP4   SLC35G1   SORBS1   TBC1D12  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_92643919)_(95471137_?)del
NC_000010.10:g.(?_94403676)_(97230894_?)del
NC_000010.9:g.(?_94393656)_(97220884_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381092,643,919 - 95,471,137CLINVAR
GRCh371094,403,676 - 97,230,894CLINVAR
Build 361094,393,656 - 97,220,884CLINVAR
Cytogenetic Map1010q23.33-24.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485470
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-11
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.