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Variant : CV155247 (GRCh38/hg38 15q13.1(chr15:28314232-28840742)x1) Homo sapiens

Symbol: CV155247
Name: GRCh38/hg38 15q13.1(chr15:28314232-28840742)x1
Condition: See cases [RCV000134859]
Clinical Significance: likely benign
Last Evaluated: 09/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: GOLGA8F   GOLGA8G   GOLGA8M   HERC2   MIR4509-2   MIR4509-3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_28314232)_(28840742_?)del
NC_000015.9:g.(?_28579796)_(29085888_?)del
NC_000015.8:g.(?_26232973)_(26884929_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381528,314,232 - 28,840,742CLINVAR
GRCh371528,579,796 - 29,085,888 (+)CLINVAR
Build 361526,232,973 - 26,884,929CLINVAR
Cytogenetic Map1515q13.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9482435
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-26
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.