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Variant : CV159245 (GRCh38/hg38 16p11.2(chr16:29581470-30179272)x1) Homo sapiens

Symbol: CV159245
Name: GRCh38/hg38 16p11.2(chr16:29581470-30179272)x1
Condition: See cases [RCV000138508]
Clinical Significance: pathogenic
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ALDOA   ALDOA   ASPHD1   C16orf54   C16orf92   CDIPT   CDIPTOSP   DOC2A   GDPD3   HIRIP3   INO80E   KCTD13   KIF22   LOC101928595   LOC112352679   LOC112352680   LOC116276452   MAPK3   MAZ   MIR3680-2   MVP   PAGR1   PPP4C   PRRT2   QPRT   SEZ6L2   SPN   TAOK2   TBX6   TLCD3B   TMEM219   YPEL3   ZG16  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000016.10:g.(?_29581470)_(30179272_?)del
NC_000016.9:g.(?_29592791)_(30190593_?)del
NC_000016.8:g.(?_29500292)_(30098094_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381629,581,470 - 30,179,272CLINVAR
GRCh371629,592,791 - 30,190,593CLINVAR
Build 361629,500,292 - 30,098,094CLINVAR
Cytogenetic Map1616p11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9486050
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.