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Variant : CV160139 (GRCh38/hg38 16p11.2(chr16:29579233-30320693)x3) Homo sapiens

Symbol: CV160139
Name: GRCh38/hg38 16p11.2(chr16:29579233-30320693)x3
Condition: See cases [RCV000139248]
Clinical Significance: likely pathogenic
Last Evaluated: 10/10/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ALDOA   ALDOA   ASPHD1   BOLA2B   C16orf54   C16orf92   CDIPT   CDIPTOSP   CORO1A   DOC2A   GDPD3   HIRIP3   INO80E   KCTD13   KIF22   LOC101928595   LOC112352679   LOC112352680   LOC116276452   MAPK3   MAZ   MIR3680-2   MVP   NPIPB13   PAGR1   PPP4C   PRRT2   QPRT   SEZ6L2   SLX1A   SLX1A-SULT1A3   SPN   SULT1A3   TAOK2   TBX6   TLCD3B   TMEM219   YPEL3   ZG16  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000016.10:g.(?_29579233)_(30320693_?)dup
Human AssemblyChrPosition (strand)Source
GRCh381629,579,233 - 30,320,693CLINVAR
GRCh371629,590,554 - 30,332,014CLINVAR
Build 361629,498,055 - 30,239,515CLINVAR
Cytogenetic Map1616p11.2CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 9486779
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-11-17
Status: ACTIVE


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