C36386Level 3

Chromosome 1 Abnormality

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** An irregularity in the structure of chromosome 1.

**Synonyms:** - Aberrant Chromosome 1

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C131489ABL2 Gene Rearrangement

C150705MTOR Gene Rearrangement

C157626Chromosome Arm 1p Loss of Heterozygosity

C168759t(1;11)(q21;q23)

C174475t(1;16)(p34;p11)

C174476t(1;22)(p34;q12)

C177205Loss of Chromosome 1q

C178352TGFBR3 Gene Rearrangement

C186798ARID1A Gene Rearrangement

C186799ARNT Gene Rearrangement

C186804BCL10 Gene Rearrangement

C186809BCL9 Gene Rearrangement

C186816CAMTA1 Gene Rearrangement

C186850EPS15 Gene Rearrangement

C186857FCGR2B Gene Rearrangement

C186858FCRL4 Gene Rearrangement

C186891JAK1 Gene Rearrangement

C186907MDS2 Gene Rearrangement

C186920MUC1 Gene Rearrangement

C186928NOTCH2 Gene Rearrangement

C186940PAX7 Gene Rearrangement

C186941PBX1 Gene Rearrangement

C186945PDE4DIP Gene Rearrangement

C186955PRDM16 Gene Rearrangement

C186956PRRX1 Gene Rearrangement

C186965RBM15 Gene Rearrangement

C186969RPL22 Gene Rearrangement

C186990SYK Gene Rearrangement

C186992TAL1 Gene Rearrangement

C187009TPM3 Gene Rearrangement

C187432GLIS1 Gene Rearrangement

C190879MEF2D Gene Rearrangement

C198829t(1;17)(q42.3;q21.2)

C199593t(1;10)(p22-31;q24-25)

C36359t(1;7)(p33;q35)

C36378t(1;12)(p36;q13-15)

C36379t(1;12)(p32-34;q13-15)

C36388t(1;2)(p11;q35-36)

C36474Ring Chromosome 1

C36501Loss of Chromosome 1p

C36521Partial Trisomy 1q

C36597Loss of Chromosome 1

C37251t(1;22)(p36.1;q12)

C37873t(X;1)(p11.2;q21)

C37875t(X;1)(p11.2;p34)

C38351t(1;4)(q44;q12)

C41614CDKN2C Gene Deletion

C46006NTRK1 Gene Rearrangement

C790991p/19q Codeletion

Cross-system equivalences0

No cross-system equivalences mapped for this node.

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