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Variant : CV436844 (GRCh37/hg19 7q11.23(chr7:72718277-74287433)x1) Homo sapiens

Symbol: CV436844
Name: GRCh37/hg19 7q11.23(chr7:72718277-74287433)x1
Condition: See cases [RCV000510195]
Clinical Significance: pathogenic
Last Evaluated: 12/22/2014
Review Status: no assertion criteria provided
Related Genes: ABHD11   ABHD11-AS1   BAZ1B   BCL7B   BUD23   CLDN3   CLDN4   CLIP2   DNAJC30   EIF4H   ELN   FKBP6   FZD9   GTF2I   GTF2IRD1   GTF2IRD2   LAT2   LIMK1   METTL27   MIR590   MLXIPL   NCF1   NSUN5   RFC2   STX1A   TBL2   TMEM270   TRIM50   VPS37D  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37772,718,277 - 74,287,433CLINVAR
Cytogenetic Map77q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443175
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-07
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.