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Variant : CV158141 (GRCh38/hg38 Xq11.1-11.2(chrX:63253804-63911433)x3) Homo sapiens

Symbol: CV158141
Name: GRCh38/hg38 Xq11.1-11.2(chrX:63253804-63911433)x3
Condition: See cases [RCV000137464]
Clinical Significance: uncertain significance
Last Evaluated: 02/18/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARHGEF9   ARHGEF9-IT1   LINC01278   MIR1468   SPIN4  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_63253804)_(63911433_?)dup
NC_000023.10:g.(?_62473681)_(63131313_?)dup
NC_000023.9:g.(?_62390406)_(63048038_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X63,253,804 - 63,911,433CLINVAR
GRCh37X62,473,681 - 63,131,313CLINVAR
Build 36X62,390,406 - 63,048,038CLINVAR
Cytogenetic MapXXq11.1-11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485019
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-23
Status: ACTIVE



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