| RH70515 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 18 | 185.7 | | UniSTS | Human GeneMap99-GB4 RH Map | 18 | 113.73 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,599,872 - 13,599,999 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,645,616 - 13,645,743 | | UniSTS | Human Celera Assembly | 18 | 13,527,951 - 13,528,078 | | RGD | Human Genome Assembly Build 36 | 18 | 13,635,616 - 13,635,743 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| RH16027 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 18 | 111.04 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,432,888 - 13,433,071 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,478,848 - 13,479,031 | | UniSTS | Human Celera Assembly | 18 | 13,360,880 - 13,361,063 | | RGD | Human Genome Assembly Build 36 | 18 | 13,468,848 - 13,469,031 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| STS-AA001607 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 18 | 184.6 | | UniSTS | Human GeneMap99-GB4 RH Map | 18 | 109.36 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,590,322 - 13,590,595 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,636,034 - 13,636,307 | | UniSTS | Human Celera Assembly | 18 | 13,518,203 - 13,518,476 | | RGD | Human Genome Assembly Build 36 | 18 | 13,626,034 - 13,626,307 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| D18S852 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 18 | 189.9 | | UniSTS | Human Whitehead-YAC Contig Map | 18 | | | UniSTS | Human Whitehead-RH Map | 18 | 100.9 | | UniSTS | Human Stanford-G3 RH Map | 18 | 533.0 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,604,449 - 13,604,565 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,650,193 - 13,650,309 | | UniSTS | Human Celera Assembly | 18 | 13,532,528 - 13,532,644 | | RGD | Human Genome Assembly Build 36 | 18 | 13,640,193 - 13,640,309 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| WI-15670 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-RH Map | 18 | 115.5 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,604,985 - 13,605,084 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,650,729 - 13,650,828 | | UniSTS | Human Celera Assembly | 18 | 13,533,064 - 13,533,163 | | RGD | Human Genome Assembly Build 36 | 18 | 13,640,729 - 13,640,828 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| RH16149 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 18 | 13,590,523 - 13,590,681 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,636,235 - 13,636,393 | | UniSTS | Human Celera Assembly | 18 | 13,518,404 - 13,518,562 | | RGD | Human Genome Assembly Build 36 | 18 | 13,626,235 - 13,626,393 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| RH92128 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly GRCh37 | 18 | 13,501,181 - 13,501,287 | | UniSTS | Human Genome Assembly Build 36 | 18 | 13,491,181 - 13,491,287 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| RH75211 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 18 | 13,497,553 - 13,497,774 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,543,354 - 13,543,575 | | UniSTS | Human Celera Assembly | 18 | 13,425,526 - 13,425,747 | | RGD | Human Genome Assembly Build 36 | 18 | 13,533,354 - 13,533,575 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| RH79722 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 18 | 101.82 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,485,853 - 13,486,142 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,531,653 - 13,531,942 | | UniSTS | Human Celera Assembly | 18 | 13,413,826 - 13,414,115 | | RGD | Human Genome Assembly Build 36 | 18 | 13,521,653 - 13,521,942 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| SHGC-81577 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 18 | 6353.0 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,383,590 - 13,383,902 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,429,545 - 13,429,857 | | UniSTS | Human Celera Assembly | 18 | 13,311,568 - 13,311,880 | | RGD | Human Genome Assembly Build 36 | 18 | 13,419,545 - 13,419,857 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| G59896 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 18 | 6320.0 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,291,545 - 13,291,656 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,337,481 - 13,337,592 | | UniSTS | Human Celera Assembly | 18 | 13,219,506 - 13,219,617 | | RGD | Human Genome Assembly Build 36 | 18 | 13,327,481 - 13,327,592 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| D18S1074 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 18 | 13,280,206 - 13,280,307 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,326,141 - 13,326,242 | | UniSTS | Human Celera Assembly | 18 | 13,208,166 - 13,208,267 | | RGD | Human Genome Assembly Build 36 | 18 | 13,316,141 - 13,316,242 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| SHGC-146549 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 18 | 6297.0 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,193,561 - 13,193,850 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,239,977 - 13,240,266 | | UniSTS | Human Celera Assembly | 18 | 13,122,240 - 13,122,529 | | RGD | Human Genome Assembly Build 36 | 18 | 13,229,977 - 13,230,266 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| SHGC-149303 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 18 | 6334.0 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,331,296 - 13,331,637 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,377,223 - 13,377,564 | | UniSTS | Human Celera Assembly | 18 | 13,259,256 - 13,259,597 | | RGD | Human Genome Assembly Build 36 | 18 | 13,367,223 - 13,367,564 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| RH65178 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 18 | 189.9 | | UniSTS | Human GeneMap99-GB4 RH Map | 18 | 111.35 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,600,711 - 13,600,887 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,646,455 - 13,646,631 | | UniSTS | Human Celera Assembly | 18 | 13,528,790 - 13,528,966 | | RGD | Human Genome Assembly Build 36 | 18 | 13,636,455 - 13,636,631 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| G20539 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 18 | 13,606,782 - 13,606,930 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,652,526 - 13,652,674 | | UniSTS | Human Celera Assembly | 18 | 13,534,861 - 13,535,009 | | RGD | Human Genome Assembly Build 36 | 18 | 13,642,526 - 13,642,674 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| A005V34 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 18 | 186.7 | | UniSTS | Human GeneMap99-GB4 RH Map | 18 | 112.66 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,606,782 - 13,606,930 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,652,526 - 13,652,674 | | UniSTS | Human Celera Assembly | 18 | 13,534,861 - 13,535,009 | | RGD | Human Genome Assembly Build 36 | 18 | 13,642,526 - 13,642,674 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| SHGC-58439 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 18 | 6320.0 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,285,254 - 13,285,350 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,331,189 - 13,331,285 | | UniSTS | Human Celera Assembly | 18 | 13,213,214 - 13,213,310 | | RGD | Human Genome Assembly Build 36 | 18 | 13,321,189 - 13,321,285 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| RH48512 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 18 | 110.4 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,173,523 - 13,173,679 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,219,936 - 13,220,092 | | UniSTS | Human Celera Assembly | 18 | 13,102,181 - 13,102,337 | | RGD | Human Genome Assembly Build 36 | 18 | 13,209,936 - 13,210,092 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| SHGC-56441 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 18 | 13,600,163 - 13,600,352 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,645,907 - 13,646,096 | | UniSTS | Human Celera Assembly | 18 | 13,528,242 - 13,528,431 | | RGD | Human Genome Assembly Build 36 | 18 | 13,635,907 - 13,636,096 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| RH15947 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 18 | 189.9 | | UniSTS | Human GeneMap99-GB4 RH Map | 18 | 111.35 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,606,813 - 13,606,978 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,652,557 - 13,652,722 | | UniSTS | Human Celera Assembly | 18 | 13,534,892 - 13,535,057 | | RGD | Human Genome Assembly Build 36 | 18 | 13,642,557 - 13,642,722 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| WIAF-2137 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 18 | 115.5 | | UniSTS | Human Genome Assembly HuRef | 18 | 13,291,531 - 13,291,796 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,337,467 - 13,337,732 | | UniSTS | Human Celera Assembly | 18 | 13,219,492 - 13,219,757 | | RGD | Human Genome Assembly Build 36 | 18 | 13,327,467 - 13,327,732 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|
| G29169 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly HuRef | 18 | 13,497,591 - 13,497,731 | | UniSTS | Human Genome Assembly GRCh37 | 18 | 13,543,392 - 13,543,532 | | UniSTS | Human Celera Assembly | 18 | 13,425,564 - 13,425,704 | | RGD | Human Genome Assembly Build 36 | 18 | 13,533,392 - 13,533,532 | | RGD | Human Cytogenetic Map | 18 | p11.21 | | UniSTS |
|