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:5 ( 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
AutCNV0002556 5 5q21.3 gain 1 - Pinto, 2010
AutCNV0002557 5 5q22.1 loss 1 - Pinto, 2010
AutCNV0002558 5 5q22.3 loss 1 - Pinto, 2010
AutCNV0002559 5 5q22.3 loss 1 - Pinto, 2010
AutCNV0002560 5 5q23.1 gain 1 - Pinto, 2010
AutCNV0002561 5 5q23.1 loss 1 - Pinto, 2010
AutCNV0002562 5 5q23.1 loss 1 - Pinto, 2010
AutCNV0002563 5 5q23.1 loss 1 - Pinto, 2010
AutCNV0002564 5 5q23.2 gain 1 - Pinto, 2010
AutCNV0002565 5 5q33.1 gain 1 - Pinto, 2010
AutCNV0002566 5 5q35.2 gain 1 - Pinto, 2010
AutCNV0002567 5 5q35.3 gain 1 - Pinto, 2010
AutCNV0002568 5 5q35.3 loss 1 - Pinto, 2010
AutCNV0003088 5 5p15.33 gain 1 - Pinto, 2010
AutCNV0003089 5 5p15.33 loss 1 - Pinto, 2010
AutCNV0003202 5 5p15.2 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003203 5 5p15.2 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003204 5 5p14.3 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003205 5 5p14.3 loss 2 - Overlapping/Recurrent CNVs; Gai, 2011
AutCNV0003206 5 5p14.3 gain 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003207 5 5p14.2 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003208 5 5q12.1 gain 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003209 5 5q12.1 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003210 5 5q13.3 loss 1 - CNVs Only Present In Patients; Gai, 2011
AutCNV0003211 5 5q13.3 loss 1 - CNVs Only Present In Patients; Gai, 2011

Page Counts: 7/11  
First  Previous  6  7  8  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