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Variant : CV555436 (GRCh37/hg19 16p13.3(chr16:85880-1875694)x1) Homo sapiens

Symbol: CV555436
Name: GRCh37/hg19 16p13.3(chr16:85880-1875694)x1
Condition: not provided [RCV000683741]
Clinical Significance: pathogenic
Last Evaluated: 03/12/2018
Review Status: no assertion criteria provided
Related Genes: ANTKMT   ARHGDIG   AXIN1   BAIAP3   C16orf91   C1QTNF8   CACNA1H   CAPN15   CCDC154   CCDC78   CHTF18   CIAO3   CLCN7   CRAMP1   DECR2   EME2   FAM234A   FBXL16   GNG13   GNPTG   HAGH   HAGHL   HBA1   HBA2   HBM   HBQ1   HBZ   IFT140   IGFALS   JMJD8   JPT2   LMF1   LUC7L   MAPK8IP3   MCRIP2   METRN   METTL26   MPG   MRPL28   MRPS34   MSLN   NHLRC4   NME3   NME4   NPRL3   NUBP2   PDIA2   PGAP6   PIGQ   POLR3K   PRR25   PRR35   PTX4   RAB11FIP3   RAB40C   RGS11   RHBDF1   RHBDL1   RHOT2   RPUSD1   SNRNP25   SOX8   SPSB3   SSTR5   STUB1   TELO2   TMEM204   TPSAB1   TPSB2   TPSD1   TPSG1   TSR3   UBE2I   UNKL   WDR24   WDR90   WFIKKN1  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371685,880 - 1,875,694CLINVAR
Cytogenetic Map1616p13.3CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 13797482
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-01-14
Status: ACTIVE


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