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Variant : CV676833 (GRCh37/hg19 Xq11.1-13.1(chrX:61882086-69173640)x1) Homo sapiens

Symbol: CV676833
Name: GRCh37/hg19 Xq11.1-13.1(chrX:61882086-69173640)x1
Condition: not provided [RCV000849932]
Clinical Significance: pathogenic
Last Evaluated: 11/14/2017
Review Status: no assertion criteria provided
Related Genes: AMER1   AR   ARHGEF9   ASB12   EDA   EDA2R   EFNB1   FAM155B   HEPH   LAS1L   MIR223   MSN   MTMR8   OPHN1   PJA1   SPIN4   STARD8   VSIG4   YIPF6   ZC3H12B   ZC4H2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X61,882,086 - 69,173,640CLINVAR
Cytogenetic MapXXq11.1-13.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14981423
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-03-24
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.