| A009H19 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 7 | 147.2 | | UniSTS | Human GeneMap99-GB4 RH Map | 7 | 50.01 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 6,250,315 - 6,250,486 | | UniSTS | Human Genome Assembly HuRef | 7 | 6,076,064 - 6,076,235 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 6,203,959 - 6,204,130 | | UniSTS | Human Celera Assembly | 7 | 6,530,982 - 6,531,153 | | RGD | Human Genome Assembly Build 36 | 7 | 6,170,484 - 6,170,655 | | RGD | Human Cytogenetic Map | 7 | p22.1 | | UniSTS |
|
| Cda0ia03 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 7 | 153.6 | | UniSTS | Human GeneMap99-GB4 RH Map | 7 | 44.31 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 6,249,281 - 6,249,418 | | UniSTS | Human Genome Assembly HuRef | 7 | 6,075,030 - 6,075,167 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 6,202,925 - 6,203,062 | | UniSTS | Human Celera Assembly | 7 | 6,532,050 - 6,532,187 | | RGD | Human Genome Assembly Build 36 | 7 | 6,169,450 - 6,169,587 | | RGD | Human Cytogenetic Map | 7 | p22.1 | | UniSTS |
|
| RH103393 |
| Map | Chr | Position | Strand | Source |
|---|
Human GeneMap99-GB4 RH Map | 7 | 50.01 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 6,247,867 - 6,248,047 | | UniSTS | Human Genome Assembly HuRef | 7 | 6,073,616 - 6,073,796 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 6,201,511 - 6,201,691 | | UniSTS | Human Celera Assembly | 7 | 6,533,421 - 6,533,601 | | RGD | Human Genome Assembly Build 36 | 7 | 6,168,036 - 6,168,216 | | RGD | Human Cytogenetic Map | 7 | p22.1 | | UniSTS |
|
| SHGC-104885 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 7 | 3124.0 | | UniSTS | Human TNG Radiation Hybrid Map | 7 | 3121.0 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 6,345,006 - 6,345,337 | | UniSTS | Human Genome Assembly HuRef | 7 | 6,170,739 - 6,171,070 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 6,298,654 - 6,298,985 | | UniSTS | Human Celera Assembly | 7 | 6,436,127 - 6,436,458 | | RGD | Human Genome Assembly Build 36 | 7 | 6,265,179 - 6,265,510 | | RGD | Human Cytogenetic Map | 7 | p22.1 | | UniSTS |
|
| SHGC-171945 |
| Map | Chr | Position | Strand | Source |
|---|
Human TNG Radiation Hybrid Map | 7 | 3090.0 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 6,280,183 - 6,280,529 | | UniSTS | Human Genome Assembly HuRef | 7 | 6,105,962 - 6,106,308 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 6,233,827 - 6,234,173 | | UniSTS | Human Celera Assembly | 7 | 6,500,939 - 6,501,285 | | RGD | Human Genome Assembly Build 36 | 7 | 6,200,352 - 6,200,698 | | RGD | Human Cytogenetic Map | 7 | p22.1 | | UniSTS |
|
| D7S3123 |
| Map | Chr | Position | Strand | Source |
|---|
Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 6,344,999 - 6,345,166 | | UniSTS | Human Genome Assembly HuRef | 7 | 6,170,732 - 6,170,899 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 6,298,647 - 6,298,814 | | UniSTS | Human Celera Assembly | 7 | 6,436,298 - 6,436,465 | | RGD | Human Genome Assembly Build 36 | 7 | 6,265,172 - 6,265,339 | | RGD | Human Cytogenetic Map | 7 | p22.1 | | UniSTS |
|
| PSCD3_8919 |
| Map | Chr | Position | Strand | Source |
|---|
Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 6,247,735 - 6,248,604 | | UniSTS | Human Genome Assembly HuRef | 7 | 6,073,484 - 6,074,353 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 6,201,379 - 6,202,248 | | UniSTS | Human Celera Assembly | 7 | 6,532,864 - 6,533,733 | | RGD | Human Genome Assembly Build 36 | 7 | 6,167,904 - 6,168,773 | | RGD |
|
| GDB:1317150 |
| Map | Chr | Position | Strand | Source |
|---|
Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 6,304,523 - 6,304,640 | | UniSTS | Human Genome Assembly HuRef | 7 | 6,130,306 - 6,130,423 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 6,258,168 - 6,258,285 | | UniSTS | Human Celera Assembly | 7 | 6,476,827 - 6,476,944 | | RGD | Human Genome Assembly Build 36 | 7 | 6,224,693 - 6,224,810 | | RGD | Human Cytogenetic Map | 7 | p22.1 | | UniSTS |
|
| STS-W02789 |
| Map | Chr | Position | Strand | Source |
|---|
Human NCBI RH Map | 7 | 147.2 | | UniSTS | Human GeneMap99-GB4 RH Map | 7 | 52.23 | | UniSTS | Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 6,247,808 - 6,248,048 | | UniSTS | Human Genome Assembly HuRef | 7 | 6,073,557 - 6,073,797 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 6,201,452 - 6,201,692 | | UniSTS | Human Celera Assembly | 7 | 6,533,420 - 6,533,660 | | RGD | Human Genome Assembly Build 36 | 7 | 6,167,977 - 6,168,217 | | RGD | Human Cytogenetic Map | 7 | p22.1 | | UniSTS |
|
| G32542 |
| Map | Chr | Position | Strand | Source |
|---|
Human Alternate Assembly CRA_TCAGchr7v2 | 7 | 6,250,315 - 6,250,486 | | UniSTS | Human Genome Assembly HuRef | 7 | 6,076,064 - 6,076,235 | | UniSTS | Human Genome Assembly GRCh37 | 7 | 6,203,959 - 6,204,130 | | UniSTS | Human Celera Assembly | 7 | 6,530,982 - 6,531,153 | | UniSTS | Human Cytogenetic Map | 7 | p22.1 | | UniSTS |
|