GRCh38/hg38 21p11.2(chr21:7743711-7865746)x3Rat Genome Database
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Variant : CV73625 (GRCh38/hg38 21p11.2(chr21:7743711-7865746)x3) Homo sapiens

Symbol: CV73625
Name: GRCh38/hg38 21p11.2(chr21:7743711-7865746)x3
RGD ID: 8619797
Condition: See cases [RCV000052824]
Clinical Significance: uncertain significance
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: FAM243B   KCNE1B   SMIM11B   SMIM34B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000021.9:g.(?_7743711)_(7865746_?)dup
NC_000021.8:g.(?_35740918)_(35888993_?)dup
NC_000021.7:g.(?_34662788)_(34810863_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38217,743,711 - 7,865,746CLINVAR
GRCh372135,740,918 - 35,888,993CLINVAR
Build 362134,662,788 - 34,810,863CLINVAR
Cytogenetic Map2121p11.2CLINVAR



Additional References at PubMed
PMID:21844811  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000052824 CLINVAR
NCBI Gene FAM243B CLINVAR
  KCNE1B CLINVAR
  SMIM11B CLINVAR
  SMIM34B CLINVAR