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Variant : CV161133 (GRCh38/hg38 21q22.11-22.12(chr21:7743711-7865746)x3) Homo sapiens

Symbol: CV161133
Name: GRCh38/hg38 21q22.11-22.12(chr21:7743711-7865746)x3
Condition: See cases [RCV000140098]
Clinical Significance: uncertain significance
Last Evaluated: 04/30/2011
Review Status: classified by 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.(?_35734654)_(35898935_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38217,743,711 - 7,865,746 (+)CLINVAR
GRCh372135,734,654 - 35,898,935CLINVAR
Build 362134,656,524 - 34,820,805CLINVAR
Cytogenetic Map2121q22.11-22.12CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487628
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-11-17
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.