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Variant : CV162239 (GRCh38/hg38 3q29(chr3:197098993-197658495)x3) Homo sapiens

Symbol: CV162239
Name: GRCh38/hg38 3q29(chr3:197098993-197658495)x3
Condition: See cases [RCV000141029]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: BDH1   DLG1   DLG1-AS1   LINC02012   MIR4797  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_197098993)_(197658495_?)dup
NC_000003.11:g.(?_196825864)_(197385366_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh383197,098,993 - 197,658,495CLINVAR
GRCh373196,825,864 - 197,385,366CLINVAR
Build 363198,310,261 - 198,869,763CLINVAR
Cytogenetic Map33q29CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9488557
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
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.