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Variant : CV160164 (GRCh38/hg38 15q14(chr15:34334908-34671997)x1) Homo sapiens

Symbol: CV160164
Name: GRCh38/hg38 15q14(chr15:34334908-34671997)x1
Condition: See cases [RCV000139269]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: GOLGA8A   GOLGA8B   LINC02252   LPCAT4   MIR1233-1   MIR1233-2   NOP10   NUTM1   SLC12A6  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_34334908)_(34671997_?)del
NC_000015.9:g.(?_34627109)_(34964198_?)del
NC_000015.8:g.(?_32414401)_(32751490_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381534,334,908 - 34,671,997CLINVAR
GRCh371534,627,109 - 34,964,198CLINVAR
Build 361532,414,401 - 32,751,490CLINVAR
Cytogenetic Map1515q14CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9486800
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.