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Variant : CV160086 (GRCh38/hg38 15q11.2(chr15:24818426-25001476)x3) Homo sapiens

Symbol: CV160086
Name: GRCh38/hg38 15q11.2(chr15:24818426-25001476)x3
Condition: See cases [RCV000139202]
Clinical Significance: likely benign
Last Evaluated: 03/09/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: PWAR5   PWARSN   SNHG14   SNORD107   SNORD108   SNORD64   SNRPN   SNURF  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_24818426)_(25001476_?)dup
NC_000015.9:g.(?_25063573)_(25246623_?)dup
NC_000015.8:g.(?_22614666)_(22797716_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381524,818,426 - 25,001,476CLINVAR
GRCh371525,063,573 - 25,246,623CLINVAR
Build 361522,614,666 - 22,797,716CLINVAR
Cytogenetic Map1515q11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486733
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-11
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.