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Variant : CV382249 (GRCh37/hg19 9q33.3-34.3(chr9:128652785-141044751)x3) Homo sapiens

Symbol: CV382249
Name: GRCh37/hg19 9q33.3-34.3(chr9:128652785-141044751)x3
Condition: See cases [RCV000447080]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ABCA2   ABL1   ABO   ADAMTS13   ADAMTSL2   AGPAT2   AIF1L   AJM1   AK1   AK8   ANAPC2   ANGPTL2   ARRDC1   ASB6   ASS1   BARHL1   BRD3   C8G   C9orf106   C9orf116   C9orf139   C9orf16   C9orf163   C9orf50   C9orf62   C9orf78   CACFD1   CACNA1B   CAMSAP1   CARD9   CCDC183   CDK9   CEL   CERCAM   CFAP157   CFAP77   CIZ1   CLIC3   COL5A1   COQ4   CRAT   CYSRT1   DBH   DDX31   DIPK1B   DNLZ   DNM1   DOLK   DOLPP1   DPH7   DPM2   DPP7   EDF1   EGFL7   EHMT1   ENDOG   ENG   ENTPD2   ENTPD8   ENTR1   EXD3   EXOSC2   FAM102A   FAM163B   FAM166A   FAM78A   FBXW5   FCN1   FCN2   FIBCD1   FNBP1   FPGS   FUBP3   FUT7   GARNL3   GBGT1   GFI1B   GLE1   GLT6D1   GOLGA2   GPR107   GPSM1   GRIN1   GTF3C4   GTF3C5   HMCN2   IER5L   INPP5E   KCNT1   KYAT1   LAMC3   LCN1   LCN10   LCN12   LCN15   LCN2   LCN6   LCN8   LCN9   LCNL1   LHX3   LMX1B   LRRC26   LRRC8A   LRSAM1   MAMDC4   MAN1B1   MED22   MED27   MIGA2   MIR126   MIR199B   MIR2861   MRPL41   MRPS2   MVB12B   MYMK   NACC2   NAIF1   NCS1   NDOR1   NELFB   NIBAN2   NOTCH1   NOXA1   NPDC1   NRARP   NRON   NSMF   NTMT1   NTNG2   NUP188   NUP214   OBP2A   OBP2B   ODF2   OLFM1   PAEP   PAXX   PBX3   PHPT1   PHYHD1   PIP5KL1   PKN3   PLPP7   PMPCA   PNPLA7   POMT1   PPP1R26   PRDM12   PRRC2B   PRRX2   PTGDS   PTGES   PTGES2   PTPA   PTRH1   QRFP   QSOX2   RABL6   RALGDS   RALGPS1   RAPGEF1   REXO4   RNF208   RNF224   RNU6ATAC   RPL12   RPL7A   RXRA   SAPCD2   SARDH   SEC16A   SET   SETX   SH2D3C   SH3GLB2   SLC25A25   SLC27A4   SLC2A6   SLC2A8   SLC34A3   SNAPC4   SNHG7   SOHLH1   SPACA9   SPOUT1   SPTAN1   SSNA1   ST6GALNAC4   ST6GALNAC6   STKLD1   STPG3   STXBP1   SURF1   SURF2   SURF4   SURF6   SWI5   TBC1D13   TMEM141   TMEM203   TMEM210   TMEM250   TOR1A   TOR1B   TOR2A   TOR4A   TPRN   TRAF2   TRUB2   TSC1   TTC16   TTF1   TUBB4B   UAP1L1   UBAC1   UCK1   URM1   USP20   VAV2   WDR34   WDR5   ZBTB34   ZBTB43   ZDHHC12   ZER1   ZMYND19   ZNF79  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh379128,652,785 - 141,044,751CLINVAR
Cytogenetic Map99q33.3-34.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12851799
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-01-07
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.