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Variant : CV159423 (GRCh38/hg38 15q14(chr15:34334908-34549221)x3) Homo sapiens

Symbol: CV159423
Name: GRCh38/hg38 15q14(chr15:34334908-34549221)x3
Condition: See cases [RCV000138654]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: GOLGA8A   GOLGA8B   LPCAT4   MIR1233-1   MIR1233-2   NOP10   NUTM1   SLC12A6  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_34334908)_(34549221_?)dup
NC_000015.9:g.(?_34627109)_(34841422_?)dup
NC_000015.8:g.(?_32414401)_(32628714_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381534,334,908 - 34,549,221CLINVAR
GRCh371534,627,109 - 34,841,422CLINVAR
Build 361532,414,401 - 32,628,714CLINVAR
Cytogenetic Map1515q14CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9486192
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
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.