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Variant : CV164397 (GRCh38/hg38 8p23.1(chr8:8273108-12610034)x1) Homo sapiens

Symbol: CV164397
Name: GRCh38/hg38 8p23.1(chr8:8273108-12610034)x1
Condition: See cases [RCV000142710]
Clinical Significance: pathogenic
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC022784.1   AC068587.4   AC104964.1   AC105001.1   AF131215.3   AF131216.3   BLK   C8orf49   C8orf74   CLDN23   CTSB   DEFB130A   DEFB130B   DEFB134   DEFB135   DEFB136   ERI1   FAM167A   FAM167A-AS1   FAM66A   FAM66D   FAM85A   FAM86B1   FAM86B2   FDFT1   GATA4   LINC00208   MFHAS1   MIR124-1   MIR124-1HG   MIR1322   MIR4286   MIR4660   MIR597   MIR598   MSRA   MTMR9   NEIL2   PINX1   PPP1R3B   PRAG1   PRSS51   PRSS55   RP1L1   SLC35G5   SNORA99   SNORD3I   SOX7   TNKS   USP17L2   USP17L7   XKR6   ZNF705D  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_8273108)_(12610034_?)del
Human AssemblyChrPosition (strand)Source
GRCh3888,273,108 - 12,610,034CLINVAR
GRCh3788,130,630 - 12,467,543CLINVAR
Build 3688,168,040 - 12,511,914CLINVAR
Cytogenetic Map88p23.1CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 9490308
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-08-04
Status: ACTIVE


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