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Variant : CV156955 (GRCh38/hg38 15q11.2(chr15:21581401-22301831)x3) Homo sapiens

Symbol: CV156955
Name: GRCh38/hg38 15q11.2(chr15:21581401-22301831)x3
Condition: See cases [RCV000136425]
Clinical Significance: benign
Last Evaluated: 03/08/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC02203   MIR1268A   MIR3118-4   MIR5701-3   OR4M2   OR4N4   POTEB  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_21581401)_(22301831_?)dup
NC_000015.9:g.(?_22285320)_(22589782_?)dup
NC_000015.8:g.(?_19786684)_(20091146_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381521,581,401 - 22,301,831 (+)CLINVAR
GRCh371522,285,320 - 22,589,782CLINVAR
Build 361519,786,684 - 20,091,146CLINVAR
Cytogenetic Map1515q11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483986
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-12-03
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.