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Variant : CV382092 (GRCh37/hg19 10q22.3-23.2(chr10:81892411-88722952)x1) Homo sapiens

Symbol: CV382092
Name: GRCh37/hg19 10q22.3-23.2(chr10:81892411-88722952)x1
Condition: See cases [RCV000447520]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ANXA11   BMPR1A   C10orf99   CCSER2   CDHR1   DYDC1   DYDC2   GHITM   GRID1   LDB3   LINC01520   LRIT1   LRIT2   MAT1A   MIR346   MMRN2   NRG3   OPN4   PLAC9   PRXL2A   RGR   SH2D4B   SNCG   TSPAN14   WAPL  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371081,892,411 - 88,722,952CLINVAR
Cytogenetic Map1010q22.3-23.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12852236
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.