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Variant : CV157512 (GRCh38/hg38 19p13.2-13.12(chr19:11525163-14155021)x1) Homo sapiens

Symbol: CV157512
Name: GRCh38/hg38 19p13.2-13.12(chr19:11525163-14155021)x1
Condition: See cases [RCV000136909]
Clinical Significance: pathogenic
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ACP5   ADGRL1   ASF1B   BEST2   C19orf53   C19orf57   C19orf67   CACNA1A   CALR   CC2D1A   CCDC130   CNN1   DAND5   DCAF15   DHPS   DNASE2   ECSIT   ELOF1   FARSA   FARSA-AS1   FBXW9   GADD45GIP1   GCDH   GET3   GNG14   HOOK2   IER2   IL27RA   JUNB   KLF1   LYL1   MAN2B1   MAST1   MIR1199   MIR181C   MIR181D   MIR23A   MIR24-2   MIR27A   MIR5684   MIR5695   MIR6515   MIR6794   MISP3   MRI1   NACC1   NANOS3   NFIX   PALM3   PODNL1   PRDX2   PRKACA   RAD23A   RFX1   RLN3   RNASEH2A   RTBDN   SAMD1   SNORD135   SNORD41   STX10   SYCE2   TNPO2   TRIR   TRMT1   WDR83   WDR83OS   ZNF136   ZNF20   ZNF433   ZNF433-AS1   ZNF439   ZNF44   ZNF440   ZNF441   ZNF442   ZNF443   ZNF490   ZNF491   ZNF563   ZNF564   ZNF625   ZNF625-ZNF20   ZNF627   ZNF69   ZNF700   ZNF709   ZNF763   ZNF788P   ZNF791   ZNF799   ZNF823   ZNF844   ZNF878   ZSWIM4  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000019.10:g.(?_11525163)_(14155021_?)del
Human AssemblyChrPosition (strand)Source
GRCh381911,525,163 - 14,155,021CLINVAR
GRCh371911,635,978 - 14,265,833CLINVAR
Build 361911,496,978 - 14,126,833CLINVAR
Cytogenetic Map1919p13.2-13.12CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9484470
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-12
Status: ACTIVE


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