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Variant : CV381764 (GRCh37/hg19 15q25.2-26.3(chr15:85089467-102495441)x3) Homo sapiens

Symbol: CV381764
Name: GRCh37/hg19 15q25.2-26.3(chr15:85089467-102495441)x3
Condition: See cases [RCV000449119]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ABHD2   ACAN   ADAMTS17   AEN   AGBL1   AKAP13   ALDH1A3   ALPK3   ANPEP   AP3S2   ARPIN   ARPIN-AP3S2   ARRDC4   ASB7   BLM   C15orf32   CERS3   CHD2   CHSY1   CIB1   CRTC3   DET1   FAM169B   FAM174B   FANCI   FES   FURIN   GDPGP1   GOLGA6L3   HAPLN3   HDDC3   IDH2   IGF1R   IQGAP1   ISG20   KIF7   KLHL25   LINC00928   LINS1   LRRC28   LRRK1   LYSMD4   MAN2A2   MCTP2   MEF2A   MESP1   MESP2   MFGE8   MIR9-3   MRPL46   MRPS11   NGRN   NMB   NR2F2   NTRK3   OR4F15   OR4F4   OR4F6   PCSK6   PDE8A   PEX11A   PGPEP1L   PLIN1   POLG   PRC1   RCCD1   RGMA   RHCG   RLBP1   SEC11A   SELENOS   SEMA4B   SLC28A1   SLCO3A1   SNRPA1   SPATA8   ST8SIA2   SV2B   SYNM   TARSL2   TICRR   TM2D3   TTC23   UNC45A   VPS33B   WDR73   WDR93   ZNF592   ZNF710   ZNF774   ZSCAN2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.9:g.(?_85089467)_(102495441_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh371585,089,467 - 102,495,441CLINVAR
Cytogenetic Map1515q25.2-26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12853816
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.