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Variant : CV380865 (GRCh37/hg19 15q25.3-26.1(chr15:88295992-94215607)x1) Homo sapiens

Symbol: CV380865
Name: GRCh37/hg19 15q25.3-26.1(chr15:88295992-94215607)x1
Condition: See cases [RCV000448680]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ABHD2   ACAN   AEN   ANPEP   AP3S2   ARPIN   ARPIN-AP3S2   BLM   C15orf32   CHD2   CIB1   CRTC3   DET1   FAM174B   FANCI   FES   FURIN   GDPGP1   HAPLN3   HDDC3   IDH2   IQGAP1   ISG20   KIF7   LINC00928   MAN2A2   MESP1   MESP2   MFGE8   MIR9-3   MRPL46   MRPS11   NGRN   NTRK3   PEX11A   PLIN1   POLG   PRC1   RCCD1   RGMA   RHCG   RLBP1   SEMA4B   SLCO3A1   ST8SIA2   SV2B   TICRR   UNC45A   VPS33B   WDR93   ZNF710   ZNF774  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.9:g.(?_88295992)_(94215607_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh371588,295,992 - 94,215,607CLINVAR
Cytogenetic Map1515q25.3-26.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12853384
Created: 2017-04-11
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.