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Variant : CV185726 (GRCh37/hg19 Xq27.1-28(chrX:138125974-147236414)x2) Homo sapiens

Symbol: CV185726
Name: GRCh37/hg19 Xq27.1-28(chrX:138125974-147236414)x2
Condition: See cases [RCV000167566]
Clinical Significance: pathogenic
Last Evaluated: 01/20/2014
Review Status: classified by single submitter|criteria provided, single submitter
Related Genes: ATP11C   CDR1   CXorf51A   CXorf51B   CXorf66   F9   FGF13   FMR1   FMR1-AS1   FMR1NB   LDOC1   MAGEC1   MAGEC2   MAGEC3   MCF2   MIR506   MIR508   MIR509-1   MIR509-3   MIR510   SLITRK2   SLITRK4   SOX3   SPANXA1   SPANXA2   SPANXB1   SPANXC   SPANXD   SPANXN1   SPANXN2   SPANXN3   SPANXN4   UBE2NL  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37X138,125,974 - 147,236,414CLINVAR
Cytogenetic MapXXq27.1-28CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 10041674
Created: 2015-05-12
Species: Homo sapiens
Last Modified: 2019-09-06
Status: ACTIVE


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