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Variant : CV160745 (GRCh38/hg38 15q25.1(chr15:78198708-78912913)x3) Homo sapiens

Symbol: CV160745
Name: GRCh38/hg38 15q25.1(chr15:78198708-78912913)x3
Condition: See cases [RCV000139779]
Clinical Significance: likely benign
Last Evaluated: 01/25/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ACSBG1   ADAMTS7   CHRNA3   CHRNA5   CHRNB4   CRABP1   DNAJA4   HYKK   IREB2   MORF4L1   PSMA4   TRK-CTT1-2   WDR61  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_78198708)_(78912913_?)dup
NC_000015.9:g.(?_78491050)_(79205255_?)dup
NC_000015.8:g.(?_76278105)_(76992310_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381578,198,708 - 78,912,913CLINVAR
GRCh371578,491,050 - 79,205,255CLINVAR
Build 361576,278,105 - 76,992,310CLINVAR
Cytogenetic Map1515q25.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487309
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.