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Variant : CV435585 (GRCh37/hg19 7q11.23(chr7:72456604-76007380)x1) Homo sapiens

Symbol: CV435585
Name: GRCh37/hg19 7q11.23(chr7:72456604-76007380)x1
Condition: See cases [RCV000510782]
Clinical Significance: pathogenic
Last Evaluated: 11/03/2014
Review Status: no assertion criteria provided
Related Genes: ABHD11   ABHD11-AS1   BAZ1B   BCL7B   BUD23   CASTOR2   CCL24   CCL26   CLDN3   CLDN4   CLIP2   DNAJC30   EIF4H   ELN   FKBP6   FZD9   GTF2I   GTF2IRD1   GTF2IRD2   GTF2IRD2B   HIP1   HSPB1   LAT2   LIMK1   MDH2   METTL27   MIR590   MLXIPL   NCF1   NSUN5   POM121C   POR   RCC1L   RFC2   RHBDD2   SPDYE5   SRRM3   STX1A   STYXL1   TBL2   TMEM120A   TMEM270   TRIM50   TRIM73   VPS37D   YWHAG  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37772,456,604 - 76,007,380CLINVAR
Cytogenetic Map77q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443760
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-14
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.