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Variant : CV383194 (GRCh37/hg19 10q22.3-23.2(chr10:81630468-88975551)x1) Homo sapiens

Symbol: CV383194
Name: GRCh37/hg19 10q22.3-23.2(chr10:81630468-88975551)x1
Condition: See cases [RCV000447214]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ADIRF   ADIRF-AS1   AGAP11   ANXA11   BMPR1A   C10orf99   CCSER2   CDHR1   DYDC1   DYDC2   FAM25A   GHITM   GLUD1   GRID1   LDB3   LINC01520   LRIT1   LRIT2   MAT1A   MIR346   MMRN2   NRG3   OPN4   PLAC9   PRXL2A   RGR   SFTPD   SH2D4B   SHLD2   SNCG   TMEM254   TSPAN14   WAPL  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371081,630,468 - 88,975,551CLINVAR
Cytogenetic Map1010q22.3-23.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12851931
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2019-12-03
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.