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Variant : CV613862 (GRCh37/hg19 10q23.33-24.1(chr10:94393383-97219175)) Homo sapiens

Symbol: CV613862
Name: GRCh37/hg19 10q23.33-24.1(chr10:94393383-97219175)
Condition: not provided [RCV000767566]
Clinical Significance: likely pathogenic
Last Evaluated: 11/01/2018
Review Status: criteria provided, single submitter
Related Genes: ACSM6   CEP55   CYP26A1   CYP26C1   CYP2C18   CYP2C19   CYP2C8   CYP2C9   EXOC6   FFAR4   FRA10AC1   HELLS   HHEX   KIF11   LGI1   MYOF   NOC3L   PDE6C   PDLIM1   PLCE1   RBP4   SLC35G1   SORBS1   TBC1D12  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371094,393,383 - 97,219,175CLINVAR
Cytogenetic Map1010q23.33-24.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14399533
Created: 2019-05-07
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.