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Variant : CV160766 (GRCh38/hg38 7q11.23(chr7:73286412-74869255)x1) Homo sapiens

Symbol: CV160766
Name: GRCh38/hg38 7q11.23(chr7:73286412-74869255)x1
Condition: See cases [RCV000139797]
Clinical Significance: pathogenic
Last Evaluated: 08/19/2011
Review Status: classified by 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   NSUN5   RFC2   STX1A   TBL2   TMEM270   TRIM50   VPS37D  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_73286412)_(74869255_?)del
NC_000007.13:g.(?_72700414)_(74285345_?)del
NC_000007.12:g.(?_72338350)_(73923281_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38773,286,412 - 74,869,255CLINVAR
GRCh37772,700,414 - 74,285,345CLINVAR
Build 36772,338,350 - 73,923,281CLINVAR
Cytogenetic Map77q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487327
Created: 2014-09-09
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.