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Variant : CV437386 (GRCh37/hg19 Xq27.3-28(chrX:146232592-155233731)x1) Homo sapiens

Symbol: CV437386
Name: GRCh37/hg19 Xq27.3-28(chrX:146232592-155233731)x1
Condition: See cases [RCV000511228]
Clinical Significance: pathogenic
Last Evaluated: 05/22/2013
Review Status: no assertion criteria provided
Related Genes: ABCD1   AFF2   ARHGAP4   ATP2B3   ATP6AP1   AVPR2   BCAP31   BGN   BRCC3   CCNQ   CD99L2   CETN2   CLIC2   CMC4   CNGA2   CSAG1   CSAG3   CTAG1A   CTAG1B   CTAG2   CXorf40A   CXorf40B   DKC1   DNASE1L1   DUSP9   EMD   F8   F8A1   F8A2   F8A3   FAM3A   FAM50A   FATE1   FLNA   FMR1   FMR1-AS1   FMR1NB   FUNDC2   G6PD   GAB3   GABRA3   GABRE   GABRQ   GDI1   GPR50   GPR50-AS1   H2AB1   H2AB2   H2AB3   HAUS7   HCFC1   HMGB3   HSFX1   HSFX2   IDH3G   IDS   IKBKG   IRAK1   L1CAM   LAGE3   MAGEA1   MAGEA10   MAGEA11   MAGEA12   MAGEA2   MAGEA2B   MAGEA3   MAGEA4   MAGEA5   MAGEA6   MAGEA8   MAGEA9   MAGEA9B   MAMLD1   MECP2   MIR105-1   MIR105-2   MIR224   MIR506   MIR508   MIR509-1   MIR509-3   MIR510   MPP1   MTCP1   MTM1   MTMR1   NAA10   NSDHL   OPN1LW   OPN1MW   OPN1MW2   PASD1   PDZD4   PLXNA3   PLXNB3   PNCK   PNMA3   PNMA5   PNMA6A   PNMA6E   PRRG3   RAB39B   RENBP   RPL10   SLC10A3   SLC6A8   SMIM9   SRPK3   SSR4   TAZ   TEX28   TKTL1   TMEM185A   TMEM187   TMLHE   TREX2   UBL4A   VBP1   VMA21   ZFP92   ZNF185   ZNF275  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X146,232,592 - 155,233,731CLINVAR
Cytogenetic MapXXq27.3-28CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13444203
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-09-06
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.