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Variant : CV159929 (GRCh38/hg38 15q13.1(chr15:28314232-28459561)x3) Homo sapiens

Symbol: CV159929
Name: GRCh38/hg38 15q13.1(chr15:28314232-28459561)x3
Condition: See cases [RCV000139068]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: GOLGA8F   HERC2   MIR4509-2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_28314232)_(28459561_?)dup
NC_000015.9:g.(?_28579796)_(28704707_?)dup
NC_000015.8:g.(?_26232973)_(26378302_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381528,314,232 - 28,459,561CLINVAR
GRCh371528,579,796 - 28,704,707 (+)CLINVAR
Build 361526,232,973 - 26,378,302CLINVAR
Cytogenetic Map1515q13.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486600
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-19
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.