Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7852
Gene Symbol: CXCR4
CXCR4 		0.010 GeneticVariation disease BEFREE CXCR4 mutations were also associated with gain of chromosome 4, gain of Xq, and deletion 6q. 26490317 2016
Entrez Id: 3342
Gene Symbol: HTC2
HTC2 		0.010 Biomarker disease BEFREE Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 --> qter) and partial monosomy 6q(6q26 --> qter) by high-resolution array CGH. 19900039 2009
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A 		0.010 GeneticVariation disease BEFREE Abnormal findings were present in 19 (83%) patients by cytogenetics/FISH/molecular analysis as follows: t(9;22) (17%); MLL gene rearrangement (26%); deletion(6q) (13%); 12p11.2 (9%); numerical abnormalities (13%), and three (13%) new, previously unreported translocations t(X;6)(p22.3;q21); t(2;6)(q37;p21.3); and t(8;14)(p21;q32). 16437134 2006
Entrez Id: 923
Gene Symbol: CD6
CD6 		0.010 GeneticVariation disease BEFREE Other karyotypic abnormalities detected were deletion 6q (40%), deletion 11 q (16.6%), deletion 7q (10%), abnormalities of chromosome 9 in (13.3%) and translocation t(11;14)(p13;q11) in 6.6% and der(12)t(12;?)(p13;?) in (3.3%). 9772908 1998
Entrez Id: 3177
Gene Symbol: SLC29A2
SLC29A2 		0.010 GeneticVariation disease BEFREE Other karyotypic abnormalities detected were deletion 6q (40%), deletion 11 q (16.6%), deletion 7q (10%), abnormalities of chromosome 9 in (13.3%) and translocation t(11;14)(p13;q11) in 6.6% and der(12)t(12;?)(p13;?) in (3.3%). 9772908 1998