| RH47897 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 2 | 224.36 | | UniSTS | Human Genome Assembly HuRef | 2 | 75,623,994 - 75,624,132 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 75,886,191 - 75,886,329 | | UniSTS | Human Celera Assembly | 2 | 75,717,471 - 75,717,609 | | RGD | Human Genome Assembly Build 36 | 2 | 75,739,699 - 75,739,837 | | RGD | Human Cytogenetic Map | 2 | p11.1-q11.2 | | UniSTS |
|
| RH99131 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 2 | 222.79 | | UniSTS | Human Genome Assembly HuRef | 2 | 75,627,474 - 75,627,590 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 75,889,671 - 75,889,787 | | UniSTS | Human Celera Assembly | 2 | 75,720,951 - 75,721,067 | | RGD | Human Genome Assembly Build 36 | 2 | 75,743,179 - 75,743,295 | | RGD | Human Cytogenetic Map | 2 | p12 | | UniSTS | Human Cytogenetic Map | 2 | p11.1-q11.2 | | UniSTS |
|
| RH25331 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 2 | 75,619,753 - 75,620,027 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 75,881,950 - 75,882,224 | | UniSTS | Human Celera Assembly | 2 | 75,713,230 - 75,713,504 | | RGD | Human Genome Assembly Build 36 | 2 | 75,735,458 - 75,735,732 | | RGD | Human Cytogenetic Map | 2 | p11.1-q11.2 | | UniSTS |
|
| RH91833 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 2 | 222.62 | | UniSTS | Human Genome Assembly HuRef | 2 | 75,622,217 - 75,622,347 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 75,884,414 - 75,884,544 | | UniSTS | Human Celera Assembly | 2 | 75,715,694 - 75,715,824 | | RGD | Human Genome Assembly Build 36 | 2 | 75,737,922 - 75,738,052 | | RGD | Human Cytogenetic Map | 2 | p11.1-q11.2 | | UniSTS |
|
| MRPL19_1324 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 2 | 75,619,996 - 75,620,779 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 75,882,193 - 75,882,976 | | UniSTS | Human Celera Assembly | 2 | 75,713,473 - 75,714,256 | | RGD | Human Genome Assembly Build 36 | 2 | 75,735,701 - 75,736,484 | | RGD |
|
| RH69443 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 2 | 222.69 | | UniSTS | Human Genome Assembly HuRef | 2 | 75,622,577 - 75,622,751 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 75,884,774 - 75,884,948 | | UniSTS | Human Celera Assembly | 2 | 75,716,054 - 75,716,228 | | RGD | Human Genome Assembly Build 36 | 2 | 75,738,282 - 75,738,456 | | RGD | Human Cytogenetic Map | 2 | p11.1-q11.2 | | UniSTS |
|
| A005D43 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-RH Map | 2 | 322.1 | | UniSTS | Human GeneMap99-GB4 RH Map | 2 | 233.33 | | UniSTS | Human Genome Assembly HuRef | 2 | 75,626,879 - 75,627,090 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 75,889,076 - 75,889,287 | | UniSTS | Human Celera Assembly | 2 | 75,720,356 - 75,720,567 | | RGD | Human Genome Assembly Build 36 | 2 | 75,742,584 - 75,742,795 | | RGD | Human Cytogenetic Map | 2 | p11.1-q11.2 | | UniSTS |
|
| SHGC-24037 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 2 | 3100.0 | | UniSTS | Human TNG Radiation Hybrid Map | 2 | 48612.0 | | UniSTS | Human Genome Assembly HuRef | 2 | 75,626,952 - 75,627,071 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 75,889,149 - 75,889,268 | | UniSTS | Human Celera Assembly | 2 | 75,720,429 - 75,720,548 | | RGD | Human Genome Assembly Build 36 | 2 | 75,742,657 - 75,742,776 | | RGD | Human Cytogenetic Map | 2 | p11.1-q11.2 | | UniSTS |
|
| RH17376 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 2 | 223.41 | | UniSTS | Human Genome Assembly HuRef | 2 | 75,620,200 - 75,620,414 | | UniSTS | Human Genome Assembly GRCh37 | 2 | 75,882,397 - 75,882,611 | | UniSTS | Human Celera Assembly | 2 | 75,713,677 - 75,713,891 | | RGD | Human Genome Assembly Build 36 | 2 | 75,735,905 - 75,736,119 | | RGD | Human Cytogenetic Map | 2 | p11.1-q11.2 | | UniSTS |
|