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Variant : CV155511 (GRCh38/hg38 22q11.22(chr22:22374043-22886630)x1) Homo sapiens

Symbol: CV155511
Name: GRCh38/hg38 22q11.22(chr22:22374043-22886630)x1
Condition: See cases [RCV000135086]
Clinical Significance: benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: GGTLC2   IGL   IGLV1-36   IGLV1-40   IGLV1-44   IGLV2-11   IGLV2-14   IGLV2-18   IGLV2-23   IGLV2-33   IGLV2-8   IGLV3-1   IGLV3-10   IGLV3-12   IGLV3-16   IGLV3-19   IGLV3-21   IGLV3-22   IGLV3-25   IGLV3-27   IGLV3-32   IGLV3-9   IGLV4-3   IGLV5-37   IGLV5-45   IGLV7-43   LL22NC03-63E9.3   MIR5571   MIR650   PRAME   ZNF280A   ZNF280B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000022.11:g.(?_22374043)_(22886630_?)del
NC_000022.10:g.(?_22728411)_(23228810_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh382222,374,043 - 22,886,630CLINVAR
GRCh372222,728,411 - 23,228,810CLINVAR
Build 362221,058,411 - 21,558,810CLINVAR
Cytogenetic Map2222q11.22CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9482659
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-08
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.