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Variant : CV380988 (GRCh37/hg19 Xq28(chrX:152886474-153368990)x2) Homo sapiens

Symbol: CV380988
Name: GRCh37/hg19 Xq28(chrX:152886474-153368990)x2
Condition: See cases [RCV000448796]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ABCD1   ARHGAP4   AVPR2   BCAP31   DUSP9   HCFC1   IDH3G   IRAK1   L1CAM   MECP2   NAA10   PDZD4   PLXNB3   PNCK   RENBP   SLC6A8   SRPK3   SSR4   TMEM187  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X152,886,474 - 153,368,990CLINVAR
Cytogenetic MapXXq28CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12853496
Created: 2017-04-11
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.