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Variant : CV155700 (GRCh38/hg38 Xq13.1(chrX:71348829-71447967)x3) Homo sapiens

Symbol: CV155700
Name: GRCh38/hg38 Xq13.1(chrX:71348829-71447967)x3
Condition: See cases [RCV000135275]
Clinical Significance: likely benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: TAF1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_71348829)_(71447967_?)dup
NC_000023.10:g.(?_70568679)_(70667817_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X71,348,829 - 71,447,967CLINVAR
GRCh37X70,568,679 - 70,667,817CLINVAR
Build 36X70,485,404 - 70,584,542CLINVAR
Cytogenetic MapXXq13.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482848
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-10-08
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.