AutismKB 2.0

View CNVs/SVs


View by Evidence Type: All ( CNVs Only Present In Patients   de novo CNVs   Overlapping/Recurrent CNVs  
                                        CNVs Overlapping With ACRD   CNVs Not Present In Control   Significant Enriched CNVs   Others  All  )


View by Chromosome:All ( 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 X  Y  All  )


Notes: ACRD: Autism Chromosome Rearrangement Database
CNV Name Chr Band Gain/Loss Number of CNVs Evidence Type Reference
Case Control
AutCNV0005057 11 - - - - CNVs Only Present In Patients; Addis L, 2015
AutCNV0005058 11 - - - - CNVs Only Present In Patients; Addis L, 2015
AutCNV0005059 11 - - - - CNVs Only Present In Patients; Addis L, 2015
AutCNV0005060 11 - - - - CNVs Only Present In Patients; Addis L, 2015
AutCNV0005061 11 - - - - CNVs Only Present In Patients; Addis L, 2015
AutCNV0005062 11 - - - - CNVs Only Present In Patients; Addis L, 2015
AutCNV0005063 11 - - - - CNVs Only Present In Patients; Addis L, 2015
AutCNV0005064 9 - gain - - CNVs Only Present In Patients; Addis L, 2015
AutCNV0005065 X - loss - - CNVs Only Present In Patients; Addis L, 2015
AutCNV0005066 X - loss - - CNVs Only Present In Patients; Chaudhry A, 2015
AutCNV0005067 X - loss - - CNVs Only Present In Patients; Chaudhry A, 2015
AutCNV0005068 X - loss - - CNVs Only Present In Patients; Chaudhry A, 2015
AutCNV0005069 X - loss - - CNVs Only Present In Patients; Chaudhry A, 2015
AutCNV0005070 X - loss - - CNVs Only Present In Patients; Chaudhry A, 2015
AutCNV0005071 X - loss - - CNVs Only Present In Patients; Chaudhry A, 2015
AutCNV0005072 X - loss - - CNVs Only Present In Patients; Chaudhry A, 2015
AutCNV0005073 X - loss - - CNVs Only Present In Patients; Chaudhry A, 2015
AutCNV0005074 X - loss - - CNVs Only Present In Patients; Chaudhry A, 2015
AutCNV0005075 X - loss - - CNVs Only Present In Patients; Chaudhry A, 2015
AutCNV0005076 X - loss - - CNVs Only Present In Patients; Chaudhry A, 2015
AutCNV0005077 X - loss - - CNVs Only Present In Patients; Chaudhry A, 2015
AutCNV0005078 X - loss - - CNVs Only Present In Patients; Chaudhry A, 2015
AutCNV0005079 16 16p13.11 gain - - CNVs Only Present In Patients; Significant Enriched CNVs; Siu WK, 2016
AutCNV0005080 15 15q11.2 loss - - CNVs Only Present In Patients; Significant Enriched CNVs; Siu WK, 2016
AutCNV0005081 15 15q23q24.1 loss - - CNVs Only Present In Patients; Significant Enriched CNVs; Siu WK, 2016

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Simple Query:


  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018