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Variant : CV556082 (GRCh37/hg19 Xq25-26.3(chrX:126759247-135790885)x1) Homo sapiens

Symbol: CV556082
Name: GRCh37/hg19 Xq25-26.3(chrX:126759247-135790885)x1
Condition: not provided [RCV000684387]
Clinical Significance: pathogenic
Last Evaluated: 11/04/2017
Review Status: no assertion criteria provided
Related Genes: ACTRT1   ADGRG4   AIFM1   APLN   ARHGAP36   ARHGEF6   BCORL1   BRS3   CCDC160   CD40LG   CT45A1   CT45A2   CT45A3   CT45A5   CT45A6   CT55   ELF4   ENOX2   FAM122B   FAM122C   FHL1   FRMD7   GPC3   GPC4   GPR119   HPRT1   HS6ST2   HTATSF1   IGSF1   INTS6L   MAP7D3   MBNL3   MIR106A   MIR19B2   MIR424   MIR503   MMGT1   MOSPD1   OCRL   OR13H1   PHF6   PLAC1   RAB33A   RAP2C   RBMX2   RTL8A   RTL8B   RTL8C   SAGE1   SASH3   SLC25A14   SLC9A6   SMARCA1   SMIM10   STK26   TFDP3   USP26   UTP14A   VGLL1   XPNPEP2   ZDHHC9   ZNF280C   ZNF449   ZNF75D  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X126,759,247 - 135,790,885CLINVAR
Cytogenetic MapXXq25-26.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798623
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-11-05
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.