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Variant : CV164802 (GRCh38/hg38 Xq27.3(chrX:143855874-144150297)x1) Homo sapiens

Symbol: CV164802
Name: GRCh38/hg38 Xq27.3(chrX:143855874-144150297)x1
Condition: See cases [RCV000143115]
Clinical Significance: likely benign
Last Evaluated: 09/27/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: UBE2NL  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_143855874)_(144150297_?)del
NC_000023.10:g.(?_142938968)_(143092138_?)del
NC_000023.9:g.(?_142766634)_(143061085_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38X143,855,874 - 144,150,297CLINVAR
GRCh37X142,938,968 - 143,092,138 (+)CLINVAR
Build 36X142,766,634 - 143,061,085CLINVAR
Cytogenetic MapXXq27.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490713
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-05
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.