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Variant : CV73834 (GRCh38/hg38 22q11.21-11.23(chr22:20726772-23135971)x1) Homo sapiens

Symbol: CV73834
Name: GRCh38/hg38 22q11.21-11.23(chr22:20726772-23135971)x1
Condition: Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053061]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053061]|See cases [RCV000053061]
Clinical Significance: pathogenic
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: AIFM3   BCRP2   BCRP4   CCDC116   CRKL   FAM230B   GGT2   GGTLC2   GNAZ   HIC2   IGL   IGLC1   IGLC2   IGLC3   IGLC7   IGLJ1   IGLJ2   IGLJ3   IGLJ4   IGLJ5   IGLJ6   IGLJ7   IGLL5   IGLV1-36   IGLV1-40   IGLV1-44   IGLV1-47   IGLV1-50   IGLV1-51   IGLV10-54   IGLV11-55   IGLV2-11   IGLV2-14   IGLV2-18   IGLV2-23   IGLV2-33   IGLV2-8   IGLV3-1   IGLV3-10   IGLV3-12   IGLV3-16   IGLV3-19   IGLV3-21   IGLV3-22   IGLV3-25   IGLV3-27   IGLV3-32   IGLV3-9   IGLV4-3   IGLV4-60   IGLV4-69   IGLV5-37   IGLV5-45   IGLV5-48   IGLV5-52   IGLV6-57   IGLV7-43   IGLV7-46   IGLV8-61   IGLV9-49   IGLVVI-22-1   LINC01637   LINC01651   LRRC74B   LZTR1   MAPK1   MIR130B   MIR301B   MIR5571   MIR649   MIR650   P2RX6   PI4KA   PPIL2   PPM1F   PRAME   PRAMENP   RIMBP3B   RIMBP3C   RSPH14   SDF2L1   SERPIND1   SLC7A4   SNAP29   THAP7   THAP7-AS1   TMEM191C   TOP3B   UBE2L3   VPREB1   YDJC   YPEL1   ZNF280A   ZNF280B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000022.11:g.(?_20726772)_(23135971_?)del
NC_000022.10:g.(?_21081060)_(23478158_?)del
NC_000022.9:g.(?_19411060)_(21808158_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh382220,726,772 - 23,135,971CLINVAR
GRCh372221,081,060 - 23,478,158CLINVAR
Build 362219,411,060 - 21,808,158CLINVAR
Cytogenetic Map2222q11.21-11.23CLINVAR
Trait Synonyms: multiple congenital anomalies; unexplained developmental delay/intellectual disability




Additional Information

 
CRRD Object Information
CRRD ID: 8620009
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2017-10-31
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.