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Variant : CV159136 (GRCh38/hg38 11q12.3(chr11:62249520-62946093)x3) Homo sapiens

Symbol: CV159136
Name: GRCh38/hg38 11q12.3(chr11:62249520-62946093)x3
Condition: See cases [RCV000138411]
Clinical Significance: pathogenic
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AHNAK   ASRGL1   B3GAT3   BSCL2   C11orf98   CHRM1   CSKMT   EEF1G   EML3   GANAB   GNG3   HNRNPUL2   HNRNPUL2-BSCL2   INTS5   LBHD1   LRRN4CL   MIR6514   MIR6747   MIR6748   MTA2   NXF1   POLR2G   ROM1   SCGB1A1   SCGB1D4   SCGB2A2   SLC3A2   SNHG1   SNORA57   SNORD22   SNORD25   SNORD26   SNORD27   SNORD28   SNORD29   SNORD30   SNORD31   STX5   TAF6L   TMEM179B   TMEM223   TTC9C   TUT1   UBXN1   UQCC3   WDR74   ZBTB3  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_62249520)_(62946093_?)dup
Human AssemblyChrPosition (strand)Source
GRCh381162,249,520 - 62,946,093CLINVAR
GRCh371162,016,992 - 62,713,565CLINVAR
Build 361161,773,568 - 62,470,141CLINVAR
Cytogenetic Map1111q12.3CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 9485958
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.