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Variant : CV157988 (GRCh38/hg38 Xq28(chrX:149804813-150311286)x4) Homo sapiens

Symbol: CV157988
Name: GRCh38/hg38 Xq28(chrX:149804813-150311286)x4
Condition: See cases [RCV000137312]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 08/05/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CXorf40B   HSFX4   LINC00850   LINC00894   MAGEA8   MAGEA8-AS1   MIR2114  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_149804813)_(150311286_?)dup
NC_000023.10:g.(?_148956425)_(149479522_?)dup
NC_000023.9:g.(?_148694272)_(149230180_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X149,804,813 - 150,311,286CLINVAR
GRCh37X148,956,425 - 149,479,522 (+)CLINVAR
Build 36X148,694,272 - 149,230,180CLINVAR
Cytogenetic MapXXq28CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484869
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-09-10
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.