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:6 ( 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
AutCNV0004868 6 6q14.1-q15 loss - - CNVs Only Present In Patients; Quintela I, 2015
AutCNV0004917 6 - loss - - CNVs Only Present In Patients; de novo CNVs; Tammimies K, 2015
AutCNV0004924 6 - loss - - CNVs Only Present In Patients; Tammimies K, 2015
AutCNV0004957 6 - gain - - CNVs Only Present In Patients; Brand H, 2015
AutCNV0005092 6 6q14.1 gain - - CNVs Only Present In Patients; Siu WK, 2016
AutCNV0005113 6 6p21.32 gain - - CNVs Only Present In Patients; de novo CNVs; Kanduri C, 2016
AutCNV0005126 6 6q26 gain - - CNVs Only Present In Patients; Yin CL, 2016
AutCNV0005127 6 6q26 gain - - CNVs Only Present In Patients; Yin CL, 2016
AutCNV0005128 6 6q26 loss - - CNVs Only Present In Patients; Yin CL, 2016
AutCNV0005129 6 6q26 loss - - CNVs Only Present In Patients; Significant Enriched CNVs; Yin CL, 2016
AutCNV0005130 6 6q26 gain - - CNVs Only Present In Patients; Significant Enriched CNVs; Yin CL, 2016
AutCNV0005131 6 6q26 loss - - CNVs Only Present In Patients; Significant Enriched CNVs; Yin CL, 2016
AutCNV0005133 6 6q22.31 - - - CNVs Only Present In Patients; Shin S, 2015
AutCNV0005624 6 6 loss - - CNVs Only Present In Patients; Mercati O, 2017
AutCNV0005653 6 6 - - - de novo CNVs; Krumm N, 2015
AutCNV0005808 6 6q24.3 Loss - - Toma C, 2014
AutCNV0005825 6 6p25.1 Loss - - Egger G, 2014
AutCNV0005826 6 "6p24.1,6p24.2" Loss - - Egger G, 2014
AutCNV0005827 6 6p22.3 Gain - - Egger G, 2014
AutCNV0005828 6 6q15 Gain - - Egger G, 2014
AutCNV0005892 6 6q13 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005893 6 6q16.1 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005894 6 6q25.3 loss - - 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