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Variant : CV156913 (GRCh38/hg38 15q11.1-11.2(chr15:20227627-22173882)x1) Homo sapiens

Symbol: CV156913
Name: GRCh38/hg38 15q11.1-11.2(chr15:20227627-22173882)x1
Condition: See cases [RCV000136383]
Clinical Significance: benign
Last Evaluated: 03/08/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FAM30C   GOLGA6L6   LINC01193   LINC02203   MIR3118-2   MIR3118-3   MIR3118-4   MIR5701-1   MIR5701-2   MIR5701-3   OR4M2   OR4N4   POTEB   POTEB2   POTEB3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_20227627)_(22173882_?)del
NC_000015.9:g.(?_20432880)_(22461833_?)del
NC_000015.8:g.(?_18692894)_(19963197_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381520,227,627 - 22,173,882CLINVAR
GRCh371520,432,880 - 22,461,833CLINVAR
Build 361518,692,894 - 19,963,197CLINVAR
Cytogenetic Map1515q11.1-11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483944
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-10-08
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.