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ChromosOmics - Database
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CHROMOSOME 10 -
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Heterochromatic
- (peri)centromeric variants
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Heterochromatic - other
heterochromatic variants |
case no.
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(molecular)
cytogenetic result
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clinical
symptoms
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reference
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10-
HHM-
acro/
1-1
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der(10)t(10;acro)(q26.3;p11.2)
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none
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{1; 26}
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Euchromatic deletions |
case no.
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(molecular)
cytogenetic result
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clinical
symptoms
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reference
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10-
EHM-del
q11.2q11.23/
1-1
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del(10)(q11.2q11.23)
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none
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{1}
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10-
EHM-del
q11.2q21.2/
1-1
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del(10)(q11.2q21.2)
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none
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{1}
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10-
EHM-del
q22.3q23.31/
1-1
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del(10)(q22.3q23.31)
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mild
to moderate
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{1}
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10-
EHM-del
q26.13qter/
1-1 to 1-2
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del(10)(q26.13)
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none
mild to moderate
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{1; 68; 77}
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10-
EHM-del
q26.13qter/
2-1 to few
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del(10)(q26.13)
reduction of signal size
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none
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{77}
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Euchromatic
duplications |
case no.
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(molecular)
cytogenetic result
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clinical
symptoms
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reference
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10-
EHM-dup
p15p14/
1-1
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dup(10)(p15p14)
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mild
to moderate
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{1}
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10-
EHM-dup
p15p13/
1-1
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dup(10)(p15p13)
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mild
to moderate
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{1}
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10-
EHM-dup
p14p13/
1-1
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dup(10)(p14p13)
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none
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{1}
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10-
EHM-dup
p11.23p11.21/
1-1
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dup(10)(p11.23p11.21)
aCGH: 30.345109-42.826062 Mb
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none
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{112}
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10-
EHM-dup
p11.22q11.22/
1-1 to few
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sSMC(10)
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none
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{sSMC
page}
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10-
EHM-dup
q26.3qter/
1-1
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dup(10)(q26.3qter)
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none
in father of affectced child
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{68}
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