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Variant : CV535482 (NC_000017.11:g.(?_16770855)_(20585863_?)del) Homo sapiens

Symbol: CV535482
Name: NC_000017.11:g.(?_16770855)_(20585863_?)del
Condition: Autistic disorder of childhood onset [RCV000754202]
Clinical Significance: pathogenic
Last Evaluated: 03/20/2018
Review Status: criteria provided, single submitter
Related Genes: AC104024.1   AKAP10   ALDH3A1   ALDH3A2   ALKBH5   ATPAF2   B9D1   CCDC144A   CDRT15L2   COPS3   DRC3   DRG2   EPN2   EPN2-AS1   EPN2-IT1   EVPLL   FAM106A   FAM106B   FAM106C   FAM83G   FBXW10   FLCN   FLII   FOXO3B   GID4   GRAP   GRAPL   GRAPL-AS1   LGALS9B   LGALS9C   LINC02076   LINC02090   LLGL1   LOC102724624   LOC105371566   LOC106020709   LOC106020710   LOC108745275   LOC108745276   LOC110121461   LOC111556156   LOC112529898   LOC112529899   LOC112529900   LOC113939958   LOC388436   MAPK7   MED9   MFAP4   MIEF2   MIR1180   MIR33B   MIR6777   MIR6778   MPRIP   MYO15A   NT5M   PEMT   PLD6   PRPSAP2   RAI1   RAI1-AS1   RASD1   RNF112   SHMT1   SLC47A1   SLC47A2   SLC5A10   SMCR2   SMCR5   SMCR8   SNORA59B   SNORD3A   SNORD3B-1   SNORD3B-2   SNORD3C   SNORD3D   SPECC1   SREBF1   TBC1D28   TNFRSF13B   TOM1L2   TOP3A   TRG-CCC3-1   TRIM16L   TRW-CCA2-1   TVP23B   ULK2  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: research
HGVS Name(s): NC_000017.11:g.(?_16770855)_(20585863_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381716,770,855 - 20,585,863CLINVAR
Cytogenetic Map1717p11.2CLINVAR



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14351773
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-09-22
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.