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Variant : CV555989 (GRCh37/hg19 Xp22.11-21.1(chrX:24650157-31844543)x2) Homo sapiens

Symbol: CV555989
Name: GRCh37/hg19 Xp22.11-21.1(chrX:24650157-31844543)x2
Condition: not provided [RCV000684294]
Clinical Significance: pathogenic
Last Evaluated: 09/29/2017
Review Status: no assertion criteria provided
Related Genes: ARX   CXorf21   DCAF8L1   DCAF8L2   DMD   FTHL17   GK   IL1RAPL1   MAGEB1   MAGEB10   MAGEB18   MAGEB2   MAGEB3   MAGEB4   MAGEB5   MAGEB6   NR0B1   PCYT1B   POLA1   TAB3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X24,650,157 - 31,844,543CLINVAR
Cytogenetic MapXXp22.11-21.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798419
Created: 2018-10-09
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.