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:All ( 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
AutCNV0004352 16 16q22.1-q22.3 loss 1 - Overlapping/Recurrent CNVs; Sanders, 2011
AutCNV0004353 16 16q22.3 gain 1 - Overlapping/Recurrent CNVs; Sanders, 2011
AutCNV0004354 16 16q23.1 loss 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004355 16 16q23.2-q24.1 loss 1 - Overlapping/Recurrent CNVs; Sanders, 2011
AutCNV0004356 16 16q23.3 loss 1 - Overlapping/Recurrent CNVs; Sanders, 2011
AutCNV0004357 16 16q23.3 loss 1 - Overlapping/Recurrent CNVs; Sanders, 2011
AutCNV0004358 16 16q24.3 loss 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004359 17 17p13.1-p13.2 gain 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004360 17 17q12 loss 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004361 17 17q12 gain 1 - de novo CNVs; Sanders, 2011
AutCNV0004362 17 17q22 loss 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004363 17 17q25.3 gain 1 - de novo CNVs; Sanders, 2011
AutCNV0004364 17 17q25.3 loss 1 - de novo CNVs; Sanders, 2011
AutCNV0004365 18 18q21.1 loss 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004366 18 18q21.32-q23 loss 1 - Overlapping/Recurrent CNVs; Sanders, 2011
AutCNV0004367 18 18q22.1 loss 1 - Overlapping/Recurrent CNVs; Sanders, 2011
AutCNV0004368 19 19p13.3 loss 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004369 19 19p13.12 gain 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004370 19 19p12 loss 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004371 19 19q13.12 loss 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004372 19 19q13.42 loss 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004373 20 20p13 loss 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004374 20 20p13 loss 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004375 20 20p12.3 loss 1 - CNVs Only Present In Patients; Sanders, 2011
AutCNV0004376 20 20p12.1 loss 1 - Overlapping/Recurrent CNVs; de novo CNVs; Sanders, 2011

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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