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Variant : CV223682 (GRCh37/hg19 7q11.23(chr7:72722981-74141840)x1) Homo sapiens

Symbol: CV223682
Name: GRCh37/hg19 7q11.23(chr7:72722981-74141840)x1
Condition: See cases [RCV000207450]
Clinical Significance: pathogenic
Last Evaluated: 02/02/2016
Review Status: criteria provided, single submitter
Related Genes: ABHD11   ABHD11-AS1   BAZ1B   BCL7B   BUD23   CLDN3   CLDN4   CLIP2   DNAJC30   EIF4H   ELN   FKBP6   FZD9   GTF2I   GTF2IRD1   LAT2   LIMK1   METTL27   MIR590   MLXIPL   RFC2   STX1A   TBL2   TMEM270   TRIM50   VPS37D  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37772,722,981 - 74,141,840CLINVAR
Cytogenetic Map77q11.23CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 11039824
Created: 2016-03-08
Species: Homo sapiens
Last Modified: 2020-01-14
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.