AutismKB 2.0

View CNVs/SVs


View by Evidence Type: de novo CNVs ( 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
AutCNV0000140 5 5p15.33-15.2 loss 1 - de novo CNVs; Marshall, 2008
AutCNV0000141 5 5p15.31-15.2 loss 1 - de novo CNVs; Marshall, 2008
AutCNV0000329 5 5p15.2 loss - - de novo CNVs; Harvard, 2005
AutCNV0000662 5 5q14.3 loss 1 - Overlapping/Recurrent CNVs; de novo CNVs; Novara, 2010
AutCNV0001487 5 5q34 loss 1 - de novo CNVs; Pinto, 2010
AutCNV0003812 5 5p15.2 loss 1 - de novo CNVs; Levy, 2011
AutCNV0004553 5 5q13.2 Loss 1 - de novo CNVs; Patircia, 2011
AutCNV0004582 5 5q13.2 Loss 1 - de novo CNVs; Patircia, 2011
AutCNV0004583 5 5q13.2 Loss 1 - de novo CNVs; Patircia, 2011
AutCNV0004584 5 5q13.2 Loss 1 - de novo CNVs; Patircia, 2011
AutCNV0004840 5 5p15.2 loss - - CNVs Only Present In Patients; de novo CNVs; Asadollahi R, 2014
AutCNV0005157 5 - loss - - CNVs Only Present In Patients; de novo CNVs; Ba W, 2016
AutCNV0005887 5 5q13.3 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005888 5 5q15 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005889 5 5q31.2 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005890 5 5q32 loss - - de novo CNVs; Brandler WM, 2018
AutCNV0005891 5 5q35.3 loss - - de novo CNVs; Brandler WM, 2018

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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