Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV383771 (GRCh37/hg19 6q26-27(chr6:164361517-170919482)x1) Homo sapiens

Symbol: CV383771
Name: GRCh37/hg19 6q26-27(chr6:164361517-170919482)x1
Condition: See cases [RCV000446024]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: AFDN   C6orf118   C6orf120   CCR6   CEP43   DACT2   DLL1   ERMARD   FAM120B   FRMD1   GPR31   KIF25   LINC02487   MPC1   PDCD2   PDE10A   PHF10   PRR18   PSMB1   RNASET2   RPS6KA2   SDIM1   SFT2D1   SMOC2   TBP   TBXT   TCTE3   THBS2   TTLL2   UNC93A   WDR27  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh376164,361,517 - 170,919,482CLINVAR
Cytogenetic Map66q26-27CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 12850753
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-06-30
Status: ACTIVE


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