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Variant : CV603487 (GRCh37/hg19 9q34.3(chr9:137816459-141114095)x1) Homo sapiens

Symbol: CV603487
Name: GRCh37/hg19 9q34.3(chr9:137816459-141114095)x1
Condition: not provided [RCV000748787]
Clinical Significance: pathogenic
Last Evaluated: 02/01/2012
Review Status: no assertion criteria provided
Related Genes: ABCA2   AGPAT2   AJM1   ANAPC2   ARRDC1   C8G   C9orf116   C9orf139   C9orf163   C9orf62   CACNA1B   CAMSAP1   CARD9   CCDC183   CLIC3   CYSRT1   DIPK1B   DNLZ   DPH7   DPP7   EDF1   EGFL7   EHMT1   ENTPD2   ENTPD8   ENTR1   EXD3   FAM157B   FAM166A   FBXW5   FUT7   GLT6D1   GPSM1   GRIN1   INPP5E   KCNT1   LCN1   LCN10   LCN12   LCN15   LCN6   LCN8   LCN9   LCNL1   LHX3   LRRC26   MAMDC4   MAN1B1   MIR126   MRPL41   MRPS2   NACC2   NDOR1   NELFB   NOTCH1   NOXA1   NPDC1   NRARP   NSMF   OBP2A   OLFM1   PAEP   PAXX   PHPT1   PMPCA   PNPLA7   PPP1R26   PTGDS   QSOX2   RABL6   RNF208   RNF224   SAPCD2   SEC16A   SLC34A3   SNAPC4   SNHG7   SOHLH1   SSNA1   STPG3   TMEM141   TMEM203   TMEM210   TMEM250   TOR4A   TPRN   TRAF2   TUBB4B   UAP1L1   UBAC1   ZMYND19  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh379137,816,459 - 141,114,095CLINVAR
Cytogenetic Map99q34.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14364120
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-14
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.