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Variant : CV159326 (GRCh38/hg38 17p11.2(chr17:17331511-19017784)x3) Homo sapiens

Symbol: CV159326
Name: GRCh38/hg38 17p11.2(chr17:17331511-19017784)x3
Condition: See cases [RCV000138572]
Clinical Significance: uncertain significance
Last Evaluated: 10/07/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ALKBH5   ATPAF2   DRC3   DRG2   EVPLL   FAM106A   FAM83G   FBXW10   FLII   GID4   LGALS9C   LINC02076   LLGL1   MED9   MIEF2   MIR33B   MIR6777   MIR6778   MYO15A   NOS2P2   NT5M   PEMT   PRPSAP2   RAI1   RAI1-AS1   RASD1   SHMT1   SLC5A10   SMCR2   SMCR5   SMCR8   SREBF1   TBC1D28   TOM1L2   TOP3A   TRIM16L   TVP23B   ZNF286B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000017.11:g.(?_17331511)_(19017784_?)dup
NC_000017.10:g.(?_17234825)_(18921097_?)dup
NC_000017.9:g.(?_17175550)_(18861822_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381717,331,511 - 19,017,784CLINVAR
GRCh371717,234,825 - 18,921,097CLINVAR
Build 361717,175,550 - 18,861,822CLINVAR
Cytogenetic Map1717p11.2CLINVAR




Additional Information

 
RGD Object Information
RGD ID: 9486112
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2016-05-31
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.