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Variant : CV159217 (GRCh38/hg38 15q11.2(chr15:25073275-25088727)x1) Homo sapiens

Symbol: CV159217
Name: GRCh38/hg38 15q11.2(chr15:25073275-25088727)x1
Condition: See cases [RCV000138481]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: SNHG14   SNORD116-10   SNORD116-11   SNORD116-12   SNORD116-13   SNORD116-14   SNORD116-15   SNORD116-16   SNORD116-17   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.(?_25073275)_(25088727_?)del
NC_000015.9:g.(?_25318422)_(25333874_?)del
NC_000015.8:g.(?_22869515)_(22884967_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381525,073,275 - 25,088,727CLINVAR
GRCh371525,318,422 - 25,333,874CLINVAR
Build 361522,869,515 - 22,884,967CLINVAR
Cytogenetic Map1515q11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486023
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-12
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.