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Variant : CV156094 (GRCh38/hg38 15q26.3(chr15:98764412-99075036)x3) Homo sapiens

Symbol: CV156094
Name: GRCh38/hg38 15q26.3(chr15:98764412-99075036)x3
Condition: See cases [RCV000135647]
Clinical Significance: uncertain significance
Last Evaluated: 01/27/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: IGF1R   LUNAR1   MIR4714   PGPEP1L  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_98764412)_(99075036_?)dup
NC_000015.9:g.(?_99307641)_(99529036_?)dup
NC_000015.8:g.(?_97125164)_(97435788_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381598,764,412 - 99,075,036CLINVAR
GRCh371599,307,641 - 99,529,036 (+)CLINVAR
Build 361597,125,164 - 97,435,788CLINVAR
Cytogenetic Map1515q26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483219
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-08-06
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.