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Variant : CV247887 (GRCh37/hg19 10q26.12-26.2(chr10:122239239-128203032)x1) Homo sapiens

Symbol: CV247887
Name: GRCh37/hg19 10q26.12-26.2(chr10:122239239-128203032)x1
Condition: See cases [RCV000240153]
Clinical Significance: pathogenic
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: ABRAXAS2   ACADSB   ADAM12   ARMS2   ATE1   BCCIP   BTBD16   BUB3   C10orf120   C10orf88   C10orf90   CHST15   CPXM2   CTBP2   CUZD1   DHX32   DMBT1   EDRF1   EEF1AKMT2   FAM24A   FAM24B   FAM53B   FANK1   FGFR2   GPR26   HMX2   HMX3   HTRA1   IKZF5   LHPP   MMP21   NKX1-2   NSMCE4A   OAT   PLEKHA1   PLPP4   PSTK   TACC2   TEX36   UROS   WDR11   ZRANB1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710122,239,239 - 128,203,032CLINVAR
Cytogenetic Map1010q26.12-26.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11541597
Created: 2016-10-11
Species: Homo sapiens
Last Modified: 2020-07-28
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.