| D7S499 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 7 | 2495.0 | | UniSTS | Human Whitehead-YAC Contig Map | 7 | | | UniSTS | Human Whitehead-RH Map | 7 | 220.5 | | UniSTS | Human GeneMap99-GB4 RH Map | 7 | 259.63 | | UniSTS | Human Stanford-G3 RH Map | 7 | 2495.0 | | UniSTS | Human deCODE Assembly Map | 7 | 77.39 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 55,611,701 - 55,611,944 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 55,611,726 - 55,612,002 | | UniSTS | Human Genome Assembly HuRef | 7 | 55,442,985 - 55,443,265 | | UniSTS | Human Genome Assembly HuRef | 7 | 55,442,960 - 55,443,207 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 55,607,479 - 55,607,755 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 55,607,454 - 55,607,697 | | UniSTS | Human Celera Assembly | 7 | 55,710,628 - 55,710,877 | | UniSTS | Human Celera Assembly | 7 | 55,710,653 - 55,710,935 | | RGD | Human Genome Assembly Build 36 | 7 | 55,574,973 - 55,575,249 | | RGD | Human Cytogenetic Map | 7 | p11.2 | | UniSTS | Genethon Human Genetic Map | 7 | 76.9 | | UniSTS | Marshfield Human Genetic Map | 7 | 75.98 | | UniSTS | Marshfield Human Genetic Map | 7 | 75.98 | | RGD |
|
| D7S2871 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 7 | 7175.0 | | UniSTS | Human NCBI RH Map | 7 | 829.2 | | UniSTS | Human Stanford-G3 RH Map | 7 | 6674.0 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 55,542,603 - 55,542,765 | | UniSTS | Human Genome Assembly HuRef | 7 | 55,373,881 - 55,374,043 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 55,538,324 - 55,538,486 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 148,195,919 - 148,196,081 | | UniSTS | Human Celera Assembly | 7 | 55,641,517 - 55,641,679 | | RGD | Human Genome Assembly Build 36 | 1 | 146,562,543 - 146,562,705 | | RGD | Human Cytogenetic Map | 1 | q21.2 | | UniSTS | Human Cytogenetic Map | 7 | p11.2 | | UniSTS |
|
| Cda1dc11 |
| Map | Chr | Position | Strand | Source |
|---|
Human Genome Assembly GRCh37 | 1 | 148,195,859 - 148,195,985 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 55,538,420 - 55,538,546 | | UniSTS | Human Genome Assembly Build 36 | 1 | 146,562,483 - 146,562,609 | | RGD | Human Cytogenetic Map | 1 | q21.2 | | UniSTS | Human Cytogenetic Map | 7 | p11.2 | | UniSTS |
|
| RH78018 |
| Map | Chr | Position | Strand | Source |
|---|
Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 55,542,603 - 55,542,785 | | UniSTS | Human Genome Assembly HuRef | 7 | 55,373,881 - 55,374,063 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 55,538,324 - 55,538,506 | | UniSTS | Human Genome Assembly GRCh37 | 1 | 148,195,899 - 148,196,081 | | UniSTS | Human Celera Assembly | 7 | 55,641,517 - 55,641,699 | | RGD | Human Genome Assembly Build 36 | 1 | 146,562,523 - 146,562,705 | | RGD | Human Cytogenetic Map | 7 | p11.2 | | UniSTS | Human Cytogenetic Map | 1 | q21.2 | | UniSTS |
|
| SHGC-68707 |
| Map | Chr | Position | Strand | Source |
|---|
Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 55,559,009 - 55,559,244 | | UniSTS | Human Genome Assembly HuRef | 7 | 55,390,289 - 55,390,524 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 55,554,741 - 55,554,976 | | UniSTS | Human Celera Assembly | 7 | 55,657,925 - 55,658,160 | | RGD | Human Genome Assembly Build 36 | 7 | 55,522,235 - 55,522,470 | | RGD | Human Cytogenetic Map | 7 | p11.2 | | UniSTS |
|
| SHGC-151050 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 9 | 53732.0 | | UniSTS | Human TNG Radiation Hybrid Map | 7 | 26754.0 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 55,611,732 - 55,612,024 | | UniSTS | Human Genome Assembly HuRef | 7 | 55,442,991 - 55,443,287 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 55,607,485 - 55,607,777 | | UniSTS | Human Celera Assembly | 7 | 55,710,659 - 55,710,957 | | RGD | Human Genome Assembly Build 36 | 7 | 55,574,979 - 55,575,271 | | RGD | Human Cytogenetic Map | 7 | p11.2 | | UniSTS |
|
| SHGC-79617 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 7 | 26748.0 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 55,602,426 - 55,602,702 | | UniSTS | Human Genome Assembly HuRef | 7 | 55,433,680 - 55,433,956 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 55,598,179 - 55,598,455 | | UniSTS | Human Celera Assembly | 7 | 55,701,348 - 55,701,624 | | RGD | Human Genome Assembly Build 36 | 7 | 55,565,673 - 55,565,949 | | RGD | Human Cytogenetic Map | 7 | p11.2 | | UniSTS |
|
| SHGC-63593 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 7 | 26727.0 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 55,549,983 - 55,550,136 | | UniSTS | Human Genome Assembly HuRef | 7 | 55,381,262 - 55,381,415 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 55,545,705 - 55,545,858 | | UniSTS | Human Celera Assembly | 7 | 55,648,899 - 55,649,052 | | RGD | Human Genome Assembly Build 36 | 7 | 55,513,199 - 55,513,352 | | RGD | Human Cytogenetic Map | 7 | p11.2 | | UniSTS |
|
| SHGC-30962 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 7 | 2484.0 | | UniSTS | Human Stanford-G3 RH Map | 7 | 2484.0 | | UniSTS | Human TNG Radiation Hybrid Map | 7 | 26764.0 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 55,632,384 - 55,632,492 | | UniSTS | Human Genome Assembly HuRef | 7 | 55,463,624 - 55,463,732 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 55,628,137 - 55,628,245 | | UniSTS | Human Celera Assembly | 7 | 55,731,294 - 55,731,402 | | RGD | Human Genome Assembly Build 36 | 7 | 55,595,631 - 55,595,739 | | RGD | Human Cytogenetic Map | 7 | p11.2 | | UniSTS |
|
| G17132 |
| Map | Chr | Position | Strand | Source |
|---|
Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 55,627,533 - 55,627,876 | | UniSTS | Human Genome Assembly HuRef | 7 | 55,458,772 - 55,459,115 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 55,623,286 - 55,623,629 | | UniSTS | Human Celera Assembly | 7 | 55,726,442 - 55,726,785 | | RGD | Human Genome Assembly Build 36 | 7 | 55,590,780 - 55,591,123 | | RGD | Human Cytogenetic Map | 7 | p11.2 | | UniSTS |
|
| STS-AA019598 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 7 | 259.53 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 55,550,006 - 55,550,221 | | UniSTS | Human Genome Assembly HuRef | 7 | 55,381,285 - 55,381,500 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 55,545,728 - 55,545,943 | | UniSTS | Human Celera Assembly | 7 | 55,648,922 - 55,649,137 | | RGD | Human Genome Assembly Build 36 | 7 | 55,513,222 - 55,513,437 | | RGD | Human Cytogenetic Map | 7 | p11.2 | | UniSTS |
|
| D7S499 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-G3 RH Map | 7 | 2495.0 | | UniSTS | Human GeneMap99-GB4 RH Map | 7 | 259.63 | | UniSTS | Human Stanford-G3 RH Map | 7 | 2495.0 | | UniSTS | Human Cytogenetic Map | 7 | p11.2 | | UniSTS |
|