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Variant : CV157706 (GRCh38/hg38 13q22.3-31.1(chr13:78177388-78681122)x1) Homo sapiens

Symbol: CV157706
Name: GRCh38/hg38 13q22.3-31.1(chr13:78177388-78681122)x1
Condition: See cases [RCV000137059]
Clinical Significance: benign
Last Evaluated: 10/20/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: OBI1   OBI1-AS1   POU4F1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000013.11:g.(?_78177388)_(78681122_?)del
NC_000013.10:g.(?_78751523)_(79255257_?)del
NC_000013.9:g.(?_77649524)_(78153258_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381378,177,388 - 78,681,122CLINVAR
GRCh371378,751,523 - 79,255,257CLINVAR
Build 361377,649,524 - 78,153,258CLINVAR
Cytogenetic Map1313q22.3-31.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484618
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.