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Variant : CV164798 (GRCh38/hg38 Xp11.3-11.23(chrX:47437831-47845763)x2) Homo sapiens

Symbol: CV164798
Name: GRCh38/hg38 Xp11.3-11.23(chrX:47437831-47845763)x2
Condition: See cases [RCV000143111]
Clinical Significance: uncertain significance
Last Evaluated: 03/19/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARAF   CFP   ELK1   LINC01560   MIR4769   SYN1   TIMP1   UXT   UXT-AS1   ZNF41   ZNF81  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_47437831)_(47845763_?)dup
Human AssemblyChrPosition (strand)Source
GRCh38X47,437,831 - 47,845,763CLINVAR
GRCh37X47,297,230 - 47,705,162CLINVAR
Build 36X47,182,174 - 47,590,106CLINVAR
Cytogenetic MapXXp11.3-11.23CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9490709
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE


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