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Variant : CV163464 (GRCh38/hg38 Xp22.2(chrX:15754290-16542056)x3) Homo sapiens

Symbol: CV163464
Name: GRCh38/hg38 Xp22.2(chrX:15754290-16542056)x3
Condition: See cases [RCV000142000]
Clinical Significance: uncertain significance
Last Evaluated: 08/19/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AP1S2   CA5B   GRPR   INE2   MAGEB17   ZRSR2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_15754290)_(16542056_?)dup
NC_000023.10:g.(?_15772413)_(16560179_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X15,754,290 - 16,542,056CLINVAR
GRCh37X15,772,413 - 16,560,179CLINVAR
Build 36X15,682,334 - 16,470,100CLINVAR
Cytogenetic MapXXp22.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489520
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-10-08
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.