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Variant : CV160738 (GRCh38/hg38 13q34(chr13:114272614-114298614)x1) Homo sapiens

Symbol: CV160738
Name: GRCh38/hg38 13q34(chr13:114272614-114298614)x1
Condition: See cases [RCV000139772]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CDC16   MIR4502   UPF3A  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000013.11:g.(?_114272614)_(114298614_?)del
NC_000013.10:g.(?_115038089)_(115064089_?)del
NC_000013.9:g.(?_114056191)_(114082191_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3813114,272,614 - 114,298,614CLINVAR
GRCh3713115,038,089 - 115,064,089CLINVAR
Build 3613114,056,191 - 114,082,191CLINVAR
Cytogenetic Map1313q34CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487302
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
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.