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Variant : CV550838 (NC_000023.10:g.152912867_153236360dup) Homo sapiens

Symbol: CV550838
Name: NC_000023.10:g.152912867_153236360dup
Condition: not provided [RCV000677999]
Clinical Significance: uncertain significance
Last Evaluated: 04/03/2018
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: duplication (SO:1000035)
Source: CLINVAR
Evidence: provider interpretation
HGVS Name(s): NC_000023.10:g.152912867_153236360dup
Position
Human AssemblyChrPosition (strand)Source
GRCh37X152,912,867 - 153,236,360CLINVAR
Cytogenetic MapXXq28CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13790725
Created: 2018-09-11
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.