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Variant : CV555405 (GRCh37/hg19 15q24.3-26.3(chr15:77479244-102429112)x3) Homo sapiens

Symbol: CV555405
Name: GRCh37/hg19 15q24.3-26.3(chr15:77479244-102429112)x3
Condition: not provided [RCV000683710]
Clinical Significance: pathogenic
Last Evaluated: 12/18/2017
Review Status: no assertion criteria provided
Related Genes: ABHD17C   ABHD2   ACAN   ACSBG1   ADAMTS17   ADAMTS7   ADAMTSL3   AEN   AGBL1   AKAP13   ALDH1A3   ALPK3   ANKRD34C   ANPEP   AP3B2   AP3S2   ARNT2   ARPIN   ARPIN-AP3S2   ARRDC4   ASB7   BCL2A1   BLM   BNC1   BTBD1   C15orf32   C15orf40   CEMIP   CERS3   CFAP161   CHD2   CHRNA3   CHRNA5   CHRNB4   CHSY1   CIB1   CIB2   CPEB1   CRABP1   CRTC3   CTSH   DET1   DNAJA4   EFL1   FAH   FAM169B   FAM174B   FANCI   FES   FSD2   FURIN   GDPGP1   GOLGA6L3   HAPLN3   HDDC3   HMG20A   HOMER2   HYKK   IDH2   IDH3A   IGF1R   IL16   IQGAP1   IREB2   ISG20   KIF7   KLHL25   LINC00928   LINGO1   LINS1   LRRC28   LRRK1   LYSMD4   MAN2A2   MCTP2   MEF2A   MESD   MESP1   MESP2   MEX3B   MFGE8   MINAR1   MIR184   MIR9-3   MORF4L1   MRPL46   MRPS11   MTHFS   NGRN   NMB   NR2F2   NTRK3   OR4F15   OR4F6   PCSK6   PDE8A   PEAK1   PEX11A   PGPEP1L   PLIN1   POLG   PRC1   PSMA4   RAMAC   RASGRF1   RCCD1   RGMA   RHCG   RLBP1   RPS17   SAXO2   SCARNA15   SEC11A   SELENOS   SEMA4B   SH2D7   SH3GL3   SLC28A1   SLCO3A1   SNRPA1   SPATA8   ST20   ST20-MTHFS   ST8SIA2   STARD5   SV2B   SYNM   TARSL2   TBC1D2B   TICRR   TLNRD1   TM2D3   TM6SF1   TMC3   TMED3   TTC23   UNC45A   VPS33B   WDR61   WDR73   WDR93   WHAMM   ZFAND6   ZNF592   ZNF710   ZNF774   ZSCAN2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.9:g.(?_77479244)_(102429112_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh371577,479,244 - 102,429,112CLINVAR
Cytogenetic Map1515q24.3-26.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13797574
Created: 2018-10-09
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.