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Variant : CV248328 (GRCh37/hg19 Xq28(chrX:152912867-153236360)x2) Homo sapiens

Symbol: CV248328
Name: GRCh37/hg19 Xq28(chrX:152912867-153236360)x2
Condition: See cases [RCV000239969]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: ABCD1   ARHGAP4   AVPR2   BCAP31   DUSP9   HCFC1   IDH3G   L1CAM   NAA10   PDZD4   PLXNB3   PNCK   RENBP   SLC6A8   SRPK3   SSR4  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X152,912,867 - 153,236,360CLINVAR
Cytogenetic MapXXq28CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11541447
Created: 2016-10-11
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.