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Variant : CV160243 (GRCh38/hg38 Xp22.33(chrX:3026061-3570788)x2) Homo sapiens

Symbol: CV160243
Name: GRCh38/hg38 Xp22.33(chrX:3026061-3570788)x2
Condition: See cases [RCV000139339]
Clinical Significance: uncertain significance
Last Evaluated: 10/24/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARSF   ARSH   LINC01546   MXRA5   SNORA48B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_3026061)_(3570788_?)dup
NC_000023.10:g.(?_2944102)_(3488829_?)dup
NC_000023.9:g.(?_2954102)_(3498829_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X3,026,061 - 3,570,788CLINVAR
GRCh37X2,944,102 - 3,488,829CLINVAR
Build 36X2,954,102 - 3,498,829CLINVAR
Cytogenetic MapXXp22.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486870
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.