| D7S2492 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 7 | 1234.0 | | UniSTS | Human Whitehead-YAC Contig Map | 7 | | | UniSTS | Human Stanford-G3 RH Map | 7 | 1234.0 | | UniSTS | Human deCODE Assembly Map | 7 | 48.18 | | UniSTS | Human TNG Radiation Hybrid Map | 7 | 15052.0 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 30,163,604 - 30,163,786 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 30,163,730 - 30,163,833 | | UniSTS | Human Genome Assembly HuRef | 7 | 29,996,217 - 29,996,320 | | UniSTS | Human Genome Assembly HuRef | 7 | 29,996,093 - 29,996,273 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 30,113,909 - 30,114,012 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 30,113,787 - 30,113,965 | | UniSTS | Human Celera Assembly | 7 | 30,103,169 - 30,103,349 | | RGD | Human Celera Assembly | 7 | 30,103,293 - 30,103,396 | | UniSTS | Human Genome Assembly Build 36 | 7 | 30,080,312 - 30,080,490 | | RGD | Human Cytogenetic Map | 7 | p21-p11.2 | | UniSTS | Genethon Human Genetic Map | 7 | 48.8 | | UniSTS | Marshfield Human Genetic Map | 7 | 48.15 | | UniSTS | Marshfield Human Genetic Map | 7 | 48.15 | | RGD |
|
| RH69225 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 7 | 151.92 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 30,141,760 - 30,142,007 | | UniSTS | Human Genome Assembly HuRef | 7 | 29,974,246 - 29,974,493 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 30,091,940 - 30,092,187 | | UniSTS | Human Celera Assembly | 7 | 30,081,322 - 30,081,569 | | RGD | Human Genome Assembly Build 36 | 7 | 30,058,465 - 30,058,712 | | RGD | Human Cytogenetic Map | 7 | p21-p11.2 | | UniSTS |
|
| RH92407 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 12 | 203.66 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 30,168,093 - 30,168,213 | | UniSTS | Human Genome Assembly HuRef | 12 | 42,595,292 - 42,595,412 | | UniSTS | Human Genome Assembly HuRef | 7 | 30,000,580 - 30,000,700 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 30,118,272 - 30,118,392 | | UniSTS | Human Genome Assembly GRCh37 | 12 | 45,566,948 - 45,567,068 | | UniSTS | Human Celera Assembly | 12 | 44,370,627 - 44,370,747 | | UniSTS | Human Celera Assembly | 7 | 30,107,656 - 30,107,776 | | RGD | Human Genome Assembly Build 36 | 7 | 30,084,797 - 30,084,917 | | RGD | Human Cytogenetic Map | 12 | q | | UniSTS | Human Cytogenetic Map | 7 | p21-p11.2 | | UniSTS |
|
| RH47354 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 7 | 132.45 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 30,173,900 - 30,174,020 | | UniSTS | Human Genome Assembly HuRef | 7 | 30,006,387 - 30,006,507 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 30,124,079 - 30,124,199 | | UniSTS | Human Celera Assembly | 7 | 30,113,463 - 30,113,583 | | RGD | Human Genome Assembly Build 36 | 7 | 30,090,604 - 30,090,724 | | RGD | Human Cytogenetic Map | 7 | p21-p11.2 | | UniSTS |
|
| SHGC-56012 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-RH Map | 7 | 95.9 | | UniSTS | Human GeneMap99-GB4 RH Map | 7 | 132.66 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 30,173,945 - 30,174,044 | | UniSTS | Human Genome Assembly HuRef | 7 | 30,006,432 - 30,006,531 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 30,124,124 - 30,124,223 | | UniSTS | Human Celera Assembly | 7 | 30,113,508 - 30,113,607 | | RGD | Human Genome Assembly Build 36 | 7 | 30,090,649 - 30,090,748 | | RGD | Human Cytogenetic Map | 7 | p21-p11.2 | | UniSTS |
|
| WI-17895 |
| Map | Chr | Position | Strand | Source |
|---|
Human Whitehead-RH Map | 7 | 86.1 | | UniSTS | Human GeneMap99-GB4 RH Map | 7 | 151.92 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 30,173,943 - 30,174,045 | | UniSTS | Human Genome Assembly HuRef | 7 | 30,006,430 - 30,006,532 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 30,124,122 - 30,124,224 | | UniSTS | Human Celera Assembly | 7 | 30,113,506 - 30,113,608 | | RGD | Human Genome Assembly Build 36 | 7 | 30,090,647 - 30,090,749 | | RGD | Human Cytogenetic Map | 7 | p21-p11.2 | | UniSTS |
|
| D7S2492 |
| Map | Chr | Position | Strand | Source |
|---|
Human Cytogenetic Map | 7 | p21-p11.2 | | UniSTS |
|