nsv7098700
- Organism: Homo sapiens
- Study:nstd230 (Sugimoto et al. 2023)
- Variant Type:complex chromosomal rearrangement
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:18
- Validation:Not tested
- Clinical Assertions: No
- Region Size:1
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 95 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 95 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 97 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 97 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 117 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 117 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 124 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 124 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 119 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 119 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 126 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 126 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 126 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 126 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 125 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 125 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 123 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 123 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 149 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 149 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 149 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 149 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 95 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 95 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view
Overlapping variant regions from other studies: 97 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 97 SVs from 20 studies. See in: genome view
Overlapping variant regions from other studies: 117 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 117 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 124 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 124 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 119 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 119 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view
Overlapping variant regions from other studies: 126 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 126 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 126 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 126 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 125 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 125 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 123 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 123 SVs from 26 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 149 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 149 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 149 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 149 SVs from 25 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|---|
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 170,544,516 | 170,544,516 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000003.12 | Chr3 | 170,544,545 | 170,544,545 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 22,490,792 | 22,490,792 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 22,490,795 | 22,490,795 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 22,490,836 | 22,490,836 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 22,490,842 | 22,490,842 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 22,490,914 | 22,490,914 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 22,490,920 | 22,490,920 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 22,639,659 | 22,639,659 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 22,639,666 | 22,639,666 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 73,287,865 | 73,287,865 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 73,287,884 | 73,287,884 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 61,498,612 | 61,498,612 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 61,498,612 | 61,498,612 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 62,071,439 | 62,071,439 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 62,071,454 | 62,071,454 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 63,108,224 | 63,108,224 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 63,108,335 | 63,108,335 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,138,531 | 65,138,531 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,138,617 | 65,138,617 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,138,682 | 65,138,682 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,138,726 | 65,138,726 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,246,330 | 65,246,330 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,246,366 | 65,246,366 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,247,661 | 65,247,661 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,247,750 | 65,247,750 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,431,904 | 65,431,904 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,432,247 | 65,432,247 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,432,272 | 65,432,272 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,432,280 | 65,432,280 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,432,385 | 65,432,385 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 65,432,460 | 65,432,460 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 66,064,445 | 66,064,445 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 66,064,451 | 66,064,451 | - |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 66,064,528 | 66,064,528 | + |
| nsv7098700 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000012.12 | Chr12 | 66,064,528 | 66,064,528 | - |
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 170,262,305 | 170,262,305 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000003.11 | Chr3 | 170,262,334 | 170,262,334 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 22,491,021 | 22,491,021 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 22,491,024 | 22,491,024 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 22,491,065 | 22,491,065 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 22,491,071 | 22,491,071 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 22,491,143 | 22,491,143 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 22,491,149 | 22,491,149 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 22,639,888 | 22,639,888 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 22,639,895 | 22,639,895 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 73,997,588 | 73,997,588 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 73,997,607 | 73,997,607 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 61,892,393 | 61,892,393 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 61,892,393 | 61,892,393 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 62,465,220 | 62,465,220 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 62,465,235 | 62,465,235 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 63,502,004 | 63,502,004 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 63,502,115 | 63,502,115 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,532,311 | 65,532,311 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,532,397 | 65,532,397 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,532,462 | 65,532,462 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,532,506 | 65,532,506 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,640,110 | 65,640,110 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,640,146 | 65,640,146 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,641,441 | 65,641,441 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,641,530 | 65,641,530 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,825,684 | 65,825,684 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,826,027 | 65,826,027 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,826,052 | 65,826,052 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,826,060 | 65,826,060 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,826,165 | 65,826,165 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 65,826,240 | 65,826,240 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 66,458,225 | 66,458,225 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 66,458,231 | 66,458,231 | - | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 66,458,308 | 66,458,308 | + | ||
| nsv7098700 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000012.11 | Chr12 | 66,458,308 | 66,458,308 | - |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18792500 | interchromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792507 | interchromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792506 | interchromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792512 | interchromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792511 | intrachromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792513 | interchromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792510 | interchromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792514 | interchromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792516 | interchromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792517 | interchromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792508 | intrachromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792505 | intrachromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792504 | intrachromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792502 | intrachromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792501 | intrachromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792515 | intrachromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792509 | intrachromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
| nssv18792503 | intrachromosomal translocation | FHU19-192 | Sequencing | Sequence alignment | 18 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|
| nssv18792500 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 170,544,516 | 170,544,516 | + |
| nssv18792507 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000003.12 | Chr3 | 170,544,545 | 170,544,545 | - |
| nssv18792506 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 22,490,792 | 22,490,792 | + |
| nssv18792512 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 22,490,795 | 22,490,795 | - |
| nssv18792511 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 22,490,836 | 22,490,836 | + |
| nssv18792513 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 22,490,842 | 22,490,842 | + |
| nssv18792510 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 22,490,914 | 22,490,914 | - |
| nssv18792514 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 22,490,920 | 22,490,920 | + |
| nssv18792511 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 22,639,659 | 22,639,659 | + |
| nssv18792507 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 22,639,666 | 22,639,666 | - |
| nssv18792516 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 73,287,865 | 73,287,865 | - |
| nssv18792517 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 73,287,884 | 73,287,884 | + |
| nssv18792506 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 61,498,612 | 61,498,612 | - |
| nssv18792508 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 61,498,612 | 61,498,612 | + |
| nssv18792505 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 62,071,439 | 62,071,439 | + |
| nssv18792504 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 62,071,454 | 62,071,454 | - |
| nssv18792505 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 63,108,224 | 63,108,224 | + |
| nssv18792502 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 63,108,335 | 63,108,335 | - |
| nssv18792501 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,138,531 | 65,138,531 | - |
| nssv18792514 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,138,617 | 65,138,617 | - |
| nssv18792515 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,138,682 | 65,138,682 | + |
| nssv18792513 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,138,726 | 65,138,726 | - |
| nssv18792512 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,246,330 | 65,246,330 | + |
| nssv18792508 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,246,366 | 65,246,366 | - |
| nssv18792509 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,247,661 | 65,247,661 | + |
| nssv18792503 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,247,750 | 65,247,750 | - |
| nssv18792504 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,431,904 | 65,431,904 | + |
| nssv18792501 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,432,247 | 65,432,247 | - |
| nssv18792500 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,432,272 | 65,432,272 | + |
| nssv18792515 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,432,280 | 65,432,280 | - |
| nssv18792516 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,432,385 | 65,432,385 | + |
| nssv18792502 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 65,432,460 | 65,432,460 | - |
| nssv18792503 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 66,064,445 | 66,064,445 | + |
| nssv18792509 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 66,064,451 | 66,064,451 | - |
| nssv18792510 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 66,064,528 | 66,064,528 | + |
| nssv18792517 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000012.12 | Chr12 | 66,064,528 | 66,064,528 | - |
| nssv18792500 | Submitted genomic | GRCh37 (hg19) | NC_000003.11 | Chr3 | 170,262,305 | 170,262,305 | + | ||
| nssv18792507 | Submitted genomic | GRCh37 (hg19) | NC_000003.11 | Chr3 | 170,262,334 | 170,262,334 | - | ||
| nssv18792506 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 22,491,021 | 22,491,021 | + | ||
| nssv18792512 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 22,491,024 | 22,491,024 | - | ||
| nssv18792511 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 22,491,065 | 22,491,065 | + | ||
| nssv18792513 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 22,491,071 | 22,491,071 | + | ||
| nssv18792510 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 22,491,143 | 22,491,143 | - | ||
| nssv18792514 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 22,491,149 | 22,491,149 | + | ||
| nssv18792511 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 22,639,888 | 22,639,888 | + | ||
| nssv18792507 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 22,639,895 | 22,639,895 | - | ||
| nssv18792516 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 73,997,588 | 73,997,588 | - | ||
| nssv18792517 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 73,997,607 | 73,997,607 | + | ||
| nssv18792506 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 61,892,393 | 61,892,393 | - | ||
| nssv18792508 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 61,892,393 | 61,892,393 | + | ||
| nssv18792505 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 62,465,220 | 62,465,220 | + | ||
| nssv18792504 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 62,465,235 | 62,465,235 | - | ||
| nssv18792505 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 63,502,004 | 63,502,004 | + | ||
| nssv18792502 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 63,502,115 | 63,502,115 | - | ||
| nssv18792501 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,532,311 | 65,532,311 | - | ||
| nssv18792514 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,532,397 | 65,532,397 | - | ||
| nssv18792515 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,532,462 | 65,532,462 | + | ||
| nssv18792513 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,532,506 | 65,532,506 | - | ||
| nssv18792512 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,640,110 | 65,640,110 | + | ||
| nssv18792508 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,640,146 | 65,640,146 | - | ||
| nssv18792509 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,641,441 | 65,641,441 | + | ||
| nssv18792503 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,641,530 | 65,641,530 | - | ||
| nssv18792504 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,825,684 | 65,825,684 | + | ||
| nssv18792501 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,826,027 | 65,826,027 | - | ||
| nssv18792500 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,826,052 | 65,826,052 | + | ||
| nssv18792515 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,826,060 | 65,826,060 | - | ||
| nssv18792516 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,826,165 | 65,826,165 | + | ||
| nssv18792502 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 65,826,240 | 65,826,240 | - | ||
| nssv18792503 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 66,458,225 | 66,458,225 | + | ||
| nssv18792509 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 66,458,231 | 66,458,231 | - | ||
| nssv18792510 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 66,458,308 | 66,458,308 | + | ||
| nssv18792517 | Submitted genomic | GRCh37 (hg19) | NC_000012.11 | Chr12 | 66,458,308 | 66,458,308 | - |