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Variant : CV160798 (GRCh38/hg38 15q14(chr15:34402939-34671997)x3) Homo sapiens

Symbol: CV160798
Name: GRCh38/hg38 15q14(chr15:34402939-34671997)x3
Condition: See cases [RCV000139823]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: GOLGA8A   GOLGA8B   LINC02252   MIR1233-2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_34402939)_(34671997_?)dup
NC_000015.9:g.(?_34695140)_(34964198_?)dup
NC_000015.8:g.(?_32482432)_(32751490_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381534,402,939 - 34,671,997CLINVAR
GRCh371534,695,140 - 34,964,198CLINVAR
Build 361532,482,432 - 32,751,490CLINVAR
Cytogenetic Map1515q14CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487353
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.