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Variant : CV383692 (GRCh37/hg19 Xq13.1-21.1(chrX:71316395-84337550)x3) Homo sapiens

Symbol: CV383692
Name: GRCh37/hg19 Xq13.1-21.1(chrX:71316395-84337550)x3
Condition: See cases [RCV000447565]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ABCB7   APOOL   ATP7A   ATRX   BRWD3   CDX4   CHIC1   CITED1   COX7B   CYLC1   CYSLTR1   DMRTC1   DMRTC1B   ERCC6L   FGF16   FTX   GPR174   HDAC8   HDX   HMGN5   ITM2A   JPX   LPAR4   MAGEE1   MAGEE2   MAGT1   NAP1L2   NEXMIF   NHSL2   P2RY10   PABPC1L2A   PABPC1L2B   PBDC1   PGAM4   PGK1   PHKA1   PIN4   POU3F4   RLIM   RPS4X   RPS6KA6   RTL3   RTL5   SH3BGRL   SLC16A2   TAF9B   TBX22   TENT5D   TSIX   UPRT   XIST   ZCCHC13   ZDHHC15  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X71,316,395 - 84,337,550CLINVAR
Cytogenetic MapXXq13.1-21.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12852281
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2019-09-10
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.