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Variant : CV161195 (GRCh38/hg38 1q21.3-22(chr1:155006546-155464263)x3) Homo sapiens

Symbol: CV161195
Name: GRCh38/hg38 1q21.3-22(chr1:155006546-155464263)x3
Condition: See cases [RCV000140157]
Clinical Significance: uncertain significance
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAM15   ASH1L   CLK2   DCST1   DCST1-AS1   DCST2   DPM3   EFNA1   EFNA3   EFNA4   FAM189B   FDPS   GBA   HCN3   KRTCAP2   MIR555   MIR92B   MTX1   MUC1   PKLR   RUSC1   RUSC1-AS1   SCAMP3   SLC50A1   THBS3   TRIM46   ZBTB7B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_155006546)_(155464263_?)dup
NC_000001.10:g.(?_154979022)_(155434054_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381155,006,546 - 155,464,263CLINVAR
GRCh371154,979,022 - 155,434,054CLINVAR
Build 361153,245,646 - 153,700,678CLINVAR
Cytogenetic Map11q21.3-22CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487687
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.