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Variant : CV556445 (GRCh37/hg19 Xq28(chrX:152398094-153176959)x2) Homo sapiens

Symbol: CV556445
Name: GRCh37/hg19 Xq28(chrX:152398094-153176959)x2
Condition: not provided [RCV000684736]
Clinical Significance: uncertain significance
Last Evaluated: 10/17/2017
Review Status: no assertion criteria provided
Related Genes: ABCD1   ARHGAP4   ATP2B3   AVPR2   BCAP31   BGN   CCNQ   DUSP9   HAUS7   IDH3G   L1CAM   MAGEA1   PDZD4   PLXNB3   PNCK   PNMA6E   SLC6A8   SRPK3   SSR4   TREX2   ZFP92   ZNF275  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X152,398,094 - 153,176,959CLINVAR
Cytogenetic MapXXq28CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798978
Created: 2018-10-09
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.