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Variant : CV73337 (GRCh38/hg38 Xq28(chrX:153787044-154397779)x2) Homo sapiens

Symbol: CV73337
Name: GRCh38/hg38 Xq28(chrX:153787044-154397779)x2
Condition: Coarse facial features [RCV000052528]|See cases [RCV000052528]
Clinical Significance: pathogenic
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: ARHGAP4   AVPR2   EMD   FLNA   HCFC1   HCFC1-AS1   IDH3G   IRAK1   L1CAM   MECP2   MIR3202-1   MIR3202-2   MIR718   NAA10   OPN1LW   OPN1MW   OPN1MW2   OPN1MW3   PDZD4   RENBP   SSR4   TEX28   TKTL1   TMEM187  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_153787044)_(154397779_?)dup
Human AssemblyChrPosition (strand)Source
GRCh38X153,787,044 - 154,397,779CLINVAR
GRCh37X153,333,946 - 153,626,120CLINVAR
Build 36X152,705,693 - 153,279,314CLINVAR
Cytogenetic MapXXq28CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 8619505
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-03-17
Status: ACTIVE


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