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Variant : CV71911 (GRCh38/hg38 7q11.23(chr7:73352304-74869255)x1) Homo sapiens

Symbol: CV71911
Name: GRCh38/hg38 7q11.23(chr7:73352304-74869255)x1
Condition: Global developmental delay [RCV000050999]|See cases [RCV000050999]
Clinical Significance: pathogenic
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|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   MIR10525   MIR4284   MIR590   MLXIPL   NCF1   RFC2   STX1A   TBL2   TMEM270   VPS37D  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_73352304)_(74869255_?)del
NC_000007.13:g.(?_72766313)_(74285345_?)del
NC_000007.12:g.(?_72404249)_(73923281_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38773,352,304 - 74,869,255CLINVAR
GRCh37772,766,313 - 74,285,345CLINVAR
Build 36772,404,249 - 73,923,281CLINVAR
Cytogenetic Map77q11.23CLINVAR
Prevalence: mental retardation is caused by aberrant copy numbers of subtelomeric regions in 3-8% of all cases.



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8618050
Created: 2014-05-13
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.