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Variant : CV556449 (GRCh37/hg19 Xq28(chrX:153012011-153064295)x1) Homo sapiens

Symbol: CV556449
Name: GRCh37/hg19 Xq28(chrX:153012011-153064295)x1
Condition: not provided [RCV000684740]
Clinical Significance: uncertain significance
Last Evaluated: 06/23/2017
Review Status: no assertion criteria provided
Related Genes: IDH3G   PLXNB3   SRPK3   SSR4  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X153,012,011 - 153,064,295CLINVAR
Cytogenetic MapXXq28CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798982
Created: 2018-10-09
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.