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:X ( 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
AutCNV0004473 X Xp22.32 loss - - CNVs Only Present In Patients; Nord, 2011
AutCNV0004489 X Xq21.31 loss - - CNVs Only Present In Patients; Nord, 2011
AutCNV0004492 X Xq26.1 loss - - CNVs Only Present In Patients; Nord, 2011
AutCNV0004521 X Xq21.2 loss - - CNVs Only Present In Patients; Nord, 2011
AutCNV0004536 X Xq27.3 loss - - CNVs Only Present In Patients; Nord, 2011
AutCNV0004544 X Xq28 loss - - CNVs Only Present In Patients; Nord, 2011
AutCNV0004597 X Xq12 Loss 1 - CNVs Only Present In Patients; Patircia, 2011
AutCNV0004598 X Xq28 Loss 1 - CNVs Only Present In Patients; Patircia, 2011
AutCNV0004599 X Xq28 Loss 1 - CNVs Only Present In Patients; Patircia, 2011
AutCNV0004629 X Xp21.1 loss 3 1 CNVs Only Present In Patients; Piton, 2008
AutCNV0004634 X Xp11.4 Gain - - Cai, 2008
AutCNV0004665 X - loss - - CNVs Only Present In Patients; Laplana M, 2014
AutCNV0004669 X Xq13-q21 gain - - CNVs Only Present In Patients; Wentz E, 2014
AutCNV0004682 X Xp21.1 loss - - CNVs Only Present In Patients; de novo CNVs; Gazzellone MJ, 2014
AutCNV0004683 X Xp21.1 loss - - CNVs Only Present In Patients; de novo CNVs; Gazzellone MJ, 2014
AutCNV0004684 X Xq13.2 loss - - CNVs Only Present In Patients; de novo CNVs; Gazzellone MJ, 2014
AutCNV0004829 X Xp22.32p22.2 loss 1 - CNVs Only Present In Patients; Margari L, 2014
AutCNV0004835 X Xp11.4 loss - - CNVs Only Present In Patients; de novo CNVs; Asadollahi R, 2014
AutCNV0004869 X Xp22.31 gain - - CNVs Only Present In Patients; Quintela I, 2015
AutCNV0004878 X Xp11.2 loss - - CNVs Only Present In Patients; De Wolf V, 2014
AutCNV0004879 X Xp11.2 loss - - CNVs Only Present In Patients; De Wolf V, 2014
AutCNV0004880 X Xp11.2 loss - - CNVs Only Present In Patients; De Wolf V, 2014
AutCNV0004881 X Xp11.2 loss - - CNVs Only Present In Patients; De Wolf V, 2014
AutCNV0004920 X - gain - - de novo CNVs; Tammimies K, 2015
AutCNV0004922 X - loss - - CNVs Only Present In Patients; de novo CNVs; Tammimies K, 2015

Page Counts: 8/11  
First  Previous  7  8  9  Next  Last

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