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:9 ( 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
AutCNV0000546 9 9q33.3-34.11 Loss 1 - Overlapping/Recurrent CNVs; Gregory, 2009
AutCNV0000547 9 9q34.11 Loss 1 - Overlapping/Recurrent CNVs; Gregory, 2009
AutCNV0000548 9 9q34.11 Gain 1 - Overlapping/Recurrent CNVs; Gregory, 2009
AutCNV0000549 9 9q34.12-34.2 Loss 1 - Overlapping/Recurrent CNVs; Gregory, 2009
AutCNV0000550 9 9q34.13-34.3 Loss 1 - Overlapping/Recurrent CNVs; Gregory, 2009
AutCNV0000551 9 9q34.13-34.2 Loss 1 - Overlapping/Recurrent CNVs; Gregory, 2009
AutCNV0000712 9 9q21 loss 2 1 Overlapping/Recurrent CNVs; Pagnamenta, 2011
AutCNV0000725 9 9q33.1 loss 1 - CNVs Only Present In Patients; Bremer, 2011
AutCNV0000726 9 9p24.1-p24.2 gain 1 - CNVs Only Present In Patients; Bremer, 2011
AutCNV0000731 9 9q13-q21.31 loss 1 - de novo CNVs; Bremer, 2011
AutCNV0000753 9 9q33.2 gain 1 - Pinto, 2010
AutCNV0000791 9 9q33.2 gain 1 - Pinto, 2010
AutCNV0000814 9 9p24.3 loss 1 - de novo CNVs; Pinto, 2010
AutCNV0000820 9 9p24.2-24.3 loss 1 - de novo CNVs; Pinto, 2010
AutCNV0000821 9 9p23 loss 1 - de novo CNVs; Pinto, 2010
AutCNV0000843 9 9p24.3 gain 1 - Pinto, 2010
AutCNV0000858 9 9p24.1 loss 1 - Pinto, 2010
AutCNV0000859 9 9p21.3 loss 1 - Pinto, 2010
AutCNV0000860 9 9p21.1 loss 1 - Pinto, 2010
AutCNV0000861 9 9q21.13 gain 1 - Pinto, 2010
AutCNV0000886 9 9p23 loss 1 - Pinto, 2010
AutCNV0000887 9 9q34.3 gain 1 - Pinto, 2010
AutCNV0000910 9 9q34.3 gain 1 - Pinto, 2010
AutCNV0000948 9 9p21.1 loss 1 - Pinto, 2010
AutCNV0000960 9 9p21.1 loss 1 - Pinto, 2010

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  (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