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:7 ( 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
AutCNV0005895 7 7q11.22 gain - - de novo CNVs; Brandler WM, 2018
AutCNV0005896 7 7q11.23 gain - - de novo CNVs; Brandler WM, 2018
AutCNV0005897 7 7q21.3 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005898 7 7q31.1 - - - de novo CNVs; Brandler WM, 2018
AutCNV0005899 7 7q34 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005942 7 7q11.23 gain - - de novo CNVs; Brandler WM, 2018

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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