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Variant : CV156729 (GRCh38/hg38 15q11.1-11.2(chr15:20419199-22308242)x1) Homo sapiens

Symbol: CV156729
Name: GRCh38/hg38 15q11.1-11.2(chr15:20419199-22308242)x1
Condition: See cases [RCV000136199]
Clinical Significance: benign
Last Evaluated: 02/06/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FAM30C   GOLGA6L6   LINC01193   LINC02203   MIR1268A   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.(?_20419199)_(22308242_?)del
NC_000015.9:g.(?_20624452)_(22669082_?)del
NC_000015.8:g.(?_18884466)_(20220446_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381520,419,199 - 22,308,242CLINVAR
GRCh371520,624,452 - 22,669,082CLINVAR
Build 361518,884,466 - 20,220,446CLINVAR
Cytogenetic Map1515q11.1-11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483760
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.