| D19S901 |
| Map | Chr | Position | Strand | Source |
|---|
Human deCODE Assembly Map | 19 | 24.07 | | UniSTS | Human TNG Radiation Hybrid Map | 19 | 1462.0 | | UniSTS | Human Genome Assembly HuRef | 1 | 50,392,272 - 50,392,734 | | UniSTS | Human Genome Assembly HuRef | 13 | 34,091,986 - 34,092,393 | | UniSTS | Human Genome Assembly HuRef | 19 | 7,149,672 - 7,149,830 | | UniSTS | Human Genome Assembly GRCh37 | 19 | 7,481,395 - 7,481,546 | | UniSTS | Human Genome Assembly GRCh37 | 9 | 121,508,952 - 121,509,311 | | UniSTS | Human Celera Assembly | 19 | 7,352,510 - 7,352,668 | | UniSTS | Human Celera Assembly | 9 | 92,156,647 - 92,157,006 | | RGD | Human Genome Assembly Build 36 | 9 | 120,548,773 - 120,549,132 | | RGD | Genethon Human Genetic Map | 19 | 24.7 | | UniSTS | Marshfield Human Genetic Map | 19 | 25.17 | | RGD | Marshfield Human Genetic Map | 19 | 25.17 | | UniSTS |
|
| HSC20B072 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 1 | 313.5 | | UniSTS | Human Whitehead-RH Map | 1 | 172.7 | | UniSTS | Human GeneMap99-GB4 RH Map | 1 | 151.08 | | UniSTS | Human GeneMap99-GB4 RH Map | 1 | 151.49 | | UniSTS | Human TNG Radiation Hybrid Map | 1 | 28169.0 | | UniSTS | Human Genome Assembly HuRef | 1 | 50,371,581 - 50,371,925 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 52,254,944 - 52,255,288 | | UniSTS | Human Celera Assembly | 1 | 50,541,482 - 50,541,826 | | RGD | Human Genome Assembly Build 36 | 1 | 52,027,532 - 52,027,876 | | RGD | Human Cytogenetic Map | 1 | p32.3 | | UniSTS | Human Cytogenetic Map | 1 | p32.2-p32.1 | | UniSTS |
|
| RH11811 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 1 | 151.49 | | UniSTS | Human Genome Assembly HuRef | 1 | 50,371,643 - 50,371,900 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 52,255,006 - 52,255,263 | | UniSTS | Human Celera Assembly | 1 | 50,541,544 - 50,541,801 | | RGD | Human Genome Assembly Build 36 | 1 | 52,027,594 - 52,027,851 | | RGD | Human Cytogenetic Map | 1 | p32.3 | | UniSTS | Human Cytogenetic Map | 1 | p32.2-p32.1 | | UniSTS |
|
| SHGC-79752 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 1 | 28196.0 | | UniSTS | Human Genome Assembly HuRef | 1 | 50,402,507 - 50,402,784 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 52,285,776 - 52,286,053 | | UniSTS | Human Celera Assembly | 1 | 50,572,392 - 50,572,669 | | RGD | Human Genome Assembly Build 36 | 1 | 52,058,364 - 52,058,641 | | RGD | Human Cytogenetic Map | 1 | p32.2-p32.1 | | UniSTS |
|
| RH123564 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 1 | 28204.0 | | UniSTS | Human Genome Assembly HuRef | 1 | 50,402,511 - 50,402,781 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 52,285,780 - 52,286,050 | | UniSTS | Human Celera Assembly | 1 | 50,572,396 - 50,572,666 | | RGD | Human Genome Assembly Build 36 | 1 | 52,058,368 - 52,058,638 | | RGD | Human Cytogenetic Map | 1 | p32.2-p32.1 | | UniSTS |
|
| SHGC-147508 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 1 | 28288.0 | | UniSTS | Human Genome Assembly HuRef | 1 | 50,433,746 - 50,434,019 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 52,317,090 - 52,317,363 | | UniSTS | Human Celera Assembly | 1 | 50,603,707 - 50,603,980 | | RGD | Human Genome Assembly Build 36 | 1 | 52,089,678 - 52,089,951 | | RGD | Human Cytogenetic Map | 1 | p32.2-p32.1 | | UniSTS |
|
| D1S3636 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 1 | 50,371,567 - 50,371,730 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 52,254,930 - 52,255,093 | | UniSTS | Human Celera Assembly | 1 | 50,541,468 - 50,541,631 | | RGD | Human Genome Assembly Build 36 | 1 | 52,027,518 - 52,027,681 | | RGD | Human Cytogenetic Map | 1 | p32.2-p32.1 | | UniSTS |
|
| A009C22 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 1 | 151.08 | | UniSTS | Human Genome Assembly HuRef | 1 | 50,411,247 - 50,411,370 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 52,294,528 - 52,294,651 | | UniSTS | Human Celera Assembly | 1 | 50,581,145 - 50,581,268 | | RGD | Human Genome Assembly Build 36 | 1 | 52,067,116 - 52,067,239 | | RGD | Human Cytogenetic Map | 1 | p32.2-p32.1 | | UniSTS |
|
| SHGC-74810 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 1 | 150.97 | | UniSTS | Human TNG Radiation Hybrid Map | 1 | 28181.0 | | UniSTS | Human Genome Assembly HuRef | 1 | 50,383,803 - 50,383,939 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 52,267,151 - 52,267,287 | | UniSTS | Human Celera Assembly | 1 | 50,553,687 - 50,553,823 | | RGD | Human Genome Assembly Build 36 | 1 | 52,039,739 - 52,039,875 | | RGD | Human Cytogenetic Map | 1 | p32.2-p32.1 | | UniSTS |
|
| SHGC-64045 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 1 | 28253.0 | | UniSTS | Human Genome Assembly HuRef | 1 | 50,421,875 - 50,421,964 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 52,305,155 - 52,305,244 | | UniSTS | Human Celera Assembly | 1 | 50,591,773 - 50,591,862 | | RGD | Human Genome Assembly Build 36 | 1 | 52,077,743 - 52,077,832 | | RGD | Human Cytogenetic Map | 1 | p32.2-p32.1 | | UniSTS |
|
| G32416 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 1 | 50,411,247 - 50,411,370 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 52,294,528 - 52,294,651 | | UniSTS | Human Celera Assembly | 1 | 50,581,145 - 50,581,268 | | UniSTS | Human Cytogenetic Map | 1 | p32.2-p32.1 | | UniSTS |
|