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Variant : CV158458 (GRCh38/hg38 9q34.11-34.12(chr9:128839676-130912873)x3) Homo sapiens

Symbol: CV158458
Name: GRCh38/hg38 9q34.11-34.12(chr9:128839676-130912873)x3
Condition: See cases [RCV000137775]
Clinical Significance: uncertain significance
Last Evaluated: 09/16/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ABL1   ASB6   ASS1   C9orf106   C9orf50   C9orf78   CRAT   DOLK   DOLPP1   EXOSC2   FIBCD1   FNBP1   FUBP3   GPR107   GPRACR   HMCN2   IER5L   KYAT1   LINC00963   LINC01503   LRRC8A   MIGA2   MIR12126   MIR6855   MIR6856   NCS1   NTMT1   NUP188   PHYHD1   PRDM12   PRRX2   PRRX2-AS1   PTGES   PTPA   QRFP   SH3GLB2   TOR1A   TOR1B   USP20  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_128839676)_(130912873_?)dup
NC_000009.11:g.(?_131601955)_(133788260_?)dup
NC_000009.10:g.(?_130641776)_(132778081_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh389128,839,676 - 130,912,873CLINVAR
GRCh379131,601,955 - 133,788,260CLINVAR
Build 369130,641,776 - 132,778,081CLINVAR
Cytogenetic Map99q34.11-34.12CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485327
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.