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Variant : CV155879 (GRCh38/hg38 Xq28(chrX:153296806-154604471)x2) Homo sapiens

Symbol: CV155879
Name: GRCh38/hg38 Xq28(chrX:153296806-154604471)x2
Condition: See cases [RCV000135451]
Clinical Significance: pathogenic
Last Evaluated: 07/30/2009
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ABCD1   ARHGAP4   ATP2B3   ATP6AP1   AVPR2   BCAP31   BGN   CCNQ   CTAG1A   DNASE1L1   DUSP9   EMD   FAM223A   FAM3A   FAM50A   FLNA   G6PD   GDI1   HAUS7   HCFC1   HCFC1-AS1   IDH3G   IKBKG   IRAK1   L1CAM   LAGE3   MECP2   MIR3202-1   MIR3202-2   MIR6858   MIR718   NAA10   OPN1LW   OPN1MW   OPN1MW2   OPN1MW3   PDZD4   PLXNA3   PLXNB3   PNCK   PNMA6E   PNMA6F   RENBP   RPL10   SLC10A3   SLC6A8   SNORA70   SRPK3   SSR4   TAZ   TEX28   TKTL1   TMEM187   TREX2   UBL4A   ZFP92   ZNF275  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_153296806)_(154604471_?)dup
Human AssemblyChrPosition (strand)Source
GRCh38X153,296,806 - 154,604,471CLINVAR
GRCh37X152,568,327 - 153,832,724 (+)CLINVAR
Build 36X152,215,458 - 153,485,918CLINVAR
Cytogenetic MapXXq28CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 9483024
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-09-10
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.