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Variant : CV160127 (GRCh38/hg38 Xq24(chrX:120666321-121243925)x3) Homo sapiens

Symbol: CV160127
Name: GRCh38/hg38 Xq24(chrX:120666321-121243925)x3
Condition: See cases [RCV000139237]
Clinical Significance: likely benign
Last Evaluated: 07/02/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CT47A1   CT47A10   CT47A11   CT47A12   CT47A2   CT47A3   CT47A4   CT47A5   CT47A6   CT47A7   CT47A8   CT47A9   CT47B1   GLUD2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_120666321)_(121243925_?)dup
NC_000023.10:g.(?_119800176)_(120377779_?)dup
NC_000023.9:g.(?_119684204)_(120205460_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X120,666,321 - 121,243,925CLINVAR
GRCh37X119,800,176 - 120,377,779CLINVAR
Build 36X119,684,204 - 120,205,460CLINVAR
Cytogenetic MapXXq24CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486768
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-31
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.