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Variant : CV160693 (GRCh38/hg38 15q11.2(chr15:20627866-22308242)x3) Homo sapiens

Symbol: CV160693
Name: GRCh38/hg38 15q11.2(chr15:20627866-22308242)x3
Condition: See cases [RCV000139734]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FAM30C   LINC01193   LINC02203   MIR1268A   MIR3118-2   MIR3118-3   MIR3118-4   MIR5701-1   MIR5701-2   MIR5701-3   OR4M2   OR4N4   POTEB   POTEB2   POTEB3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_20627866)_(22308242_?)dup
NC_000015.9:g.(?_20833169)_(22698579_?)dup
NC_000015.8:g.(?_19093183)_(20249943_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381520,627,866 - 22,308,242CLINVAR
GRCh371520,833,169 - 22,698,579CLINVAR
Build 361519,093,183 - 20,249,943CLINVAR
Cytogenetic Map1515q11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487264
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-10-15
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.