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 |
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CHROMOSOME 10 -
| Heterochromatic - centromeric - other heterochromatic variants |
Euchromatic - euchromatic deletions - euchromatic duplications |
| References | |
| case no. |
(molecular) cytogenetic result |
clinical symptoms |
reference |
| 10- cen+/ 1-1 to few |
10cen+ D10Z1 |
none |
{1 pages 68-69} |
| 10- cen-/ 1-1 to few |
10cen- D10Z1 |
none |
{1 pages 68-69} |
| 10- inv/ 1-1 to few |
inv(10)(p11.2q21.2) |
none |
{1 pages 68-69} |
| case no. |
(molecular)
cytogenetic result |
clinical
symptoms |
reference |
| 10- HHM- acro/ 1-1 |
der(10)t(10;acro)(q26.3;p11.2)
|
none |
{1; 26} |
| case no. |
(molecular)
cytogenetic result |
clinical
symptoms |
reference |
| 10- EHM-del q11.2q11.23/ 1-1 |
del(10)(q11.2q11.23) |
none |
{1} |
| 10- EHM-del q11.2q21.2/ 1-1 |
del(10)(q11.2q21.2) |
none |
{1} |
| 10- EHM-del q22.3q23.31/ 1-1 |
del(10)(q22.3q23.31) |
mild
to moderate |
{1} |
| 10- EHM-del q26.13qter/ 1-1 to 1-2 |
del(10)(q26.13) |
none mild to moderate |
{1; 68; 77} |
| 10- EHM-del q26.13qter/ 2-1 to few |
del(10)(q26.13) reduction of signal size |
none |
{77} |
| case no. |
(molecular)
cytogenetic result |
clinical
symptoms |
reference |
| 10- EHM-dup p15p14/ 1-1 |
dup(10)(p15p14) |
mild
to moderate |
{1} |
| 10- EHM-dup p15p13/ 1-1 |
dup(10)(p15p13) |
mild
to moderate |
{1} |
| 10- EHM-dup p14p13/ 1-1 |
dup(10)(p14p13) |
none |
{1} |
| 10- EHM-dup p11.23p11.21/ 1-1 |
dup(10)(p11.23p11.21) position hg19/GRCh37: 30,345,109-42,826,062 |
none |
{112} |
| 10- EHM-dup p11.23p11.22/ 1-1 |
dup(10)(p11.23p11.22) position hg19/GRCh37: 50,353,069-52,889,528 |
none
in mother and seen also in fetus |
{0} - provided from China |
| 10- EHM-dup p11.22q11.22/ 1-1 to few |
sSMC(10) |
none |
{sSMC page} |
| 10- EHM-dup q22.2q23.2/ 1-1 |
dup(10)(q22.2q23.2)
position hg19/GRCh37: 77,448,435-88,786,593 |
none |
{131} |
| 10- EHM-dup q26.3qter/ 1-1 |
dup(10)(q26.3qter) |
none
in father of affectced child |
{68} |