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Variant : CV74865 (GRCh38/hg38 19p13.13(chr19:12813597-13119698)x3) Homo sapiens

Symbol: CV74865
Name: GRCh38/hg38 19p13.13(chr19:12813597-13119698)x3
Condition: See cases [RCV000054144]
Clinical Significance: uncertain significance
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: CALR   DAND5   DNASE2   FARSA   FARSA-AS1   GADD45GIP1   GCDH   KLF1   LOC110121458   LOC112543452   LOC112543454   LOC112543455   LOC117125585   LOC117125586   LOC117125587   LOC117125588   LOC117125589   LOC117125590   LOC117125591   LOC117125592   LOC117125593   LOC117125594   LOC117125595   LOC117125596   LOC117125597   LYL1   MAST1   MIR5695   MIR6515   MIR6794   NACC1   NFIX   RAD23A   RNASEH2A   RTBDN   SYCE2   TRMT1  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000019.10:g.(?_12813597)_(13119698_?)dup
Human AssemblyChrPosition (strand)Source
GRCh381912,813,597 - 13,119,698CLINVAR
GRCh371912,924,411 - 13,230,512CLINVAR
Build 361912,785,411 - 13,091,512CLINVAR
Cytogenetic Map1919p13.13CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 8621057
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-11-17
Status: ACTIVE


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