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Variant : CV555973 (GRCh37/hg19 Xp22.2(chrX:15772413-16261761)x3) Homo sapiens

Symbol: CV555973
Name: GRCh37/hg19 Xp22.2(chrX:15772413-16261761)x3
Condition: not provided [RCV000684278]
Clinical Significance: uncertain significance
Last Evaluated: 01/30/2018
Review Status: no assertion criteria provided
Related Genes: AP1S2   CA5B   GRPR   INE2   MAGEB17   ZRSR2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X15,772,413 - 16,261,761CLINVAR
Cytogenetic MapXXp22.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798392
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-10-15
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.