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Variant : CV159135 (GRCh38/hg38 15q11.2(chr15:25084469-25088727)x1) Homo sapiens

Symbol: CV159135
Name: GRCh38/hg38 15q11.2(chr15:25084469-25088727)x1
Condition: See cases [RCV000138410]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: SNHG14   SNORD116-18   SNORD116-19   SNORD116-20   SNORD116@  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_25084469)_(25088727_?)del
NC_000015.9:g.(?_25329616)_(25333874_?)del
NC_000015.8:g.(?_22880709)_(22884967_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381525,084,469 - 25,088,727CLINVAR
GRCh371525,329,616 - 25,333,874CLINVAR
Build 361522,880,709 - 22,884,967CLINVAR
Cytogenetic Map1515q11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485957
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-11
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.