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Variant : CV163177 (GRCh38/hg38 15q11.2(chr15:25056998-25073086)x1) Homo sapiens

Symbol: CV163177
Name: GRCh38/hg38 15q11.2(chr15:25056998-25073086)x1
Condition: See cases [RCV000141816]
Clinical Significance: uncertain significance
Last Evaluated: 06/11/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: SNHG14   SNORD116-4   SNORD116-5   SNORD116-6   SNORD116-7   SNORD116-8   SNORD116@  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_25056998)_(25073086_?)del
NC_000015.9:g.(?_25302145)_(25318233_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381525,056,998 - 25,073,086CLINVAR
GRCh371525,302,145 - 25,318,233CLINVAR
Build 361522,853,238 - 22,869,326CLINVAR
Cytogenetic Map1515q11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489339
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
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.