GRCh38/hg38 21q11.2(chr21:13399449-14335064)x3Rat Genome Database
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Variant : CV155791 (GRCh38/hg38 21q11.2(chr21:13399449-14335064)x3) Homo sapiens

Symbol: CV155791
Name: GRCh38/hg38 21q11.2(chr21:13399449-14335064)x3
RGD ID: 9482939
Condition: See cases [RCV000135366]
Clinical Significance: uncertain significance
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC01674   LIPI   LOC105377134   MIR3118-1   MIR3156-3   MIR8069-2   POTED   RBM11  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000021.9:g.(?_13399449)_(14335064_?)dup
NC_000021.8:g.(?_14771770)_(15707385_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh382113,399,449 - 14,335,064CLINVAR
GRCh372114,771,770 - 15,707,385CLINVAR
Build 362113,693,641 - 14,629,256CLINVAR
Cytogenetic Map2121q11.2CLINVAR




Additional Information

Database Acc Id Source(s)
ClinVar RCV000135366 CLINVAR
NCBI Gene 102724188 CLINVAR
  105377134 CLINVAR
  LIPI CLINVAR
  MIR3118-1 CLINVAR
  MIR3156-3 CLINVAR
  MIR8069-2 CLINVAR
  POTED CLINVAR
  RBM11 CLINVAR
OMIM 607549 CLINVAR
  609252 CLINVAR
  617937 CLINVAR