nsv7098705
- Organism: Homo sapiens
- Study:nstd230 (Sugimoto et al. 2023)
- Variant Type:complex chromosomal rearrangement
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:16
- 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: 90 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 90 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 93 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 93 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 91 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 91 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 87 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 87 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 87 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 87 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 86 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 86 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 96 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 96 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 200 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 200 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 199 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 199 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 219 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 219 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 204 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 204 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 166 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 166 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 78 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 78 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 90 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 90 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 93 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 93 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 89 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 91 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 91 SVs from 16 studies. See in: genome view
Overlapping variant regions from other studies: 87 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 87 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 87 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 87 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 86 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 86 SVs from 19 studies. See in: genome view
Overlapping variant regions from other studies: 96 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 96 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 200 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 200 SVs from 22 studies. See in: genome view
Overlapping variant regions from other studies: 199 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 199 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 219 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 219 SVs from 29 studies. See in: genome view
Overlapping variant regions from other studies: 204 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 204 SVs from 23 studies. See in: genome view
Overlapping variant regions from other studies: 166 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 166 SVs from 21 studies. See in: genome view
Overlapping variant regions from other studies: 78 SVs from 18 studies. See in: genome view
Overlapping variant regions from other studies: 78 SVs from 18 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 |
|---|---|---|---|---|---|---|---|---|---|---|
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 151,977,717 | 151,977,717 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 151,977,720 | 151,977,720 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 152,139,958 | 152,139,958 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 152,139,958 | 152,139,958 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 152,369,483 | 152,369,483 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 152,369,692 | 152,369,692 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 152,371,455 | 152,371,455 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 152,371,461 | 152,371,461 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 152,371,481 | 152,371,481 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 152,371,485 | 152,371,485 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 152,376,093 | 152,376,093 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 152,376,105 | 152,376,105 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 153,190,316 | 153,190,316 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 153,190,329 | 153,190,329 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 153,190,343 | 153,190,343 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 153,190,344 | 153,190,344 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 153,300,178 | 153,300,178 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 153,300,182 | 153,300,182 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 153,542,719 | 153,542,719 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 153,542,719 | 153,542,719 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 106,962,369 | 106,962,369 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 106,962,369 | 106,962,369 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 107,004,835 | 107,004,835 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 107,004,837 | 107,004,837 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 82,161,789 | 82,161,789 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 82,161,793 | 82,161,793 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 87,265,792 | 87,265,792 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000013.11 | Chr13 | 87,265,806 | 87,265,806 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 97,967,370 | 97,967,370 | + |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000015.10 | Chr15 | 97,967,371 | 97,967,371 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 26,198,849 | 26,198,849 | - |
| nsv7098705 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000016.10 | Chr16 | 26,198,868 | 26,198,868 | + |
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 152,298,852 | 152,298,852 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 152,298,855 | 152,298,855 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 152,461,093 | 152,461,093 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 152,461,093 | 152,461,093 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 152,690,618 | 152,690,618 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 152,690,827 | 152,690,827 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 152,692,590 | 152,692,590 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 152,692,596 | 152,692,596 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 152,692,616 | 152,692,616 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 152,692,620 | 152,692,620 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 152,697,228 | 152,697,228 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 152,697,240 | 152,697,240 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 153,511,451 | 153,511,451 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 153,511,464 | 153,511,464 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 153,511,478 | 153,511,478 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 153,511,479 | 153,511,479 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 153,621,313 | 153,621,313 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 153,621,317 | 153,621,317 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 153,863,854 | 153,863,854 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 153,863,854 | 153,863,854 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 107,614,717 | 107,614,717 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 107,614,717 | 107,614,717 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 107,657,183 | 107,657,183 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 107,657,185 | 107,657,185 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 82,735,924 | 82,735,924 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 82,735,928 | 82,735,928 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 87,918,047 | 87,918,047 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000013.10 | Chr13 | 87,918,061 | 87,918,061 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 98,510,600 | 98,510,600 | + | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000015.9 | Chr15 | 98,510,601 | 98,510,601 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 26,210,170 | 26,210,170 | - | ||
| nsv7098705 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000016.9 | Chr16 | 26,210,189 | 26,210,189 | + |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| nssv18792366 | interchromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792375 | interchromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792374 | intrachromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792380 | intrachromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792379 | intrachromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792378 | interchromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792371 | interchromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792370 | intrachromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792373 | interchromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792368 | intrachromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792369 | intrachromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792367 | interchromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792384 | intrachromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792372 | interchromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792377 | interchromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
| nssv18792376 | intrachromosomal translocation | FHU15-167 | Sequencing | Sequence alignment | 16 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop | strand |
|---|---|---|---|---|---|---|---|---|---|
| nssv18792366 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 151,977,717 | 151,977,717 | + |
| nssv18792375 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 151,977,720 | 151,977,720 | - |
| nssv18792374 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 152,139,958 | 152,139,958 | + |
| nssv18792380 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 152,139,958 | 152,139,958 | - |
| nssv18792379 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 152,369,483 | 152,369,483 | - |
| nssv18792378 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 152,369,692 | 152,369,692 | + |
| nssv18792379 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 152,371,455 | 152,371,455 | + |
| nssv18792371 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 152,371,461 | 152,371,461 | - |
| nssv18792370 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 152,371,481 | 152,371,481 | + |
| nssv18792374 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 152,371,485 | 152,371,485 | - |
| nssv18792373 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 152,376,093 | 152,376,093 | + |
| nssv18792368 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 152,376,105 | 152,376,105 | - |
| nssv18792369 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 153,190,316 | 153,190,316 | - |
| nssv18792369 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 153,190,329 | 153,190,329 | + |
| nssv18792370 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 153,190,343 | 153,190,343 | + |
| nssv18792367 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 153,190,344 | 153,190,344 | - |
| nssv18792384 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 153,300,178 | 153,300,178 | - |
| nssv18792368 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 153,300,182 | 153,300,182 | + |
| nssv18792380 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 153,542,719 | 153,542,719 | + |
| nssv18792384 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 153,542,719 | 153,542,719 | - |
| nssv18792372 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 82,161,789 | 82,161,789 | - |
| nssv18792377 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 82,161,793 | 82,161,793 | + |
| nssv18792373 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 87,265,792 | 87,265,792 | + |
| nssv18792375 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 87,265,806 | 87,265,806 | - |
| nssv18792367 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 106,962,369 | 106,962,369 | - |
| nssv18792376 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 106,962,369 | 106,962,369 | + |
| nssv18792376 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 107,004,835 | 107,004,835 | - |
| nssv18792366 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000013.11 | Chr13 | 107,004,837 | 107,004,837 | + |
| nssv18792378 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 97,967,370 | 97,967,370 | + |
| nssv18792377 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000015.10 | Chr15 | 97,967,371 | 97,967,371 | - |
| nssv18792371 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 26,198,849 | 26,198,849 | - |
| nssv18792372 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000016.10 | Chr16 | 26,198,868 | 26,198,868 | + |
| nssv18792366 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 152,298,852 | 152,298,852 | + | ||
| nssv18792375 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 152,298,855 | 152,298,855 | - | ||
| nssv18792374 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 152,461,093 | 152,461,093 | + | ||
| nssv18792380 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 152,461,093 | 152,461,093 | - | ||
| nssv18792379 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 152,690,618 | 152,690,618 | - | ||
| nssv18792378 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 152,690,827 | 152,690,827 | + | ||
| nssv18792379 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 152,692,590 | 152,692,590 | + | ||
| nssv18792371 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 152,692,596 | 152,692,596 | - | ||
| nssv18792370 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 152,692,616 | 152,692,616 | + | ||
| nssv18792374 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 152,692,620 | 152,692,620 | - | ||
| nssv18792373 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 152,697,228 | 152,697,228 | + | ||
| nssv18792368 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 152,697,240 | 152,697,240 | - | ||
| nssv18792369 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 153,511,451 | 153,511,451 | - | ||
| nssv18792369 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 153,511,464 | 153,511,464 | + | ||
| nssv18792370 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 153,511,478 | 153,511,478 | + | ||
| nssv18792367 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 153,511,479 | 153,511,479 | - | ||
| nssv18792384 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 153,621,313 | 153,621,313 | - | ||
| nssv18792368 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 153,621,317 | 153,621,317 | + | ||
| nssv18792380 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 153,863,854 | 153,863,854 | + | ||
| nssv18792384 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 153,863,854 | 153,863,854 | - | ||
| nssv18792372 | Submitted genomic | GRCh37 (hg19) | NC_000013.10 | Chr13 | 82,735,924 | 82,735,924 | - | ||
| nssv18792377 | Submitted genomic | GRCh37 (hg19) | NC_000013.10 | Chr13 | 82,735,928 | 82,735,928 | + | ||
| nssv18792373 | Submitted genomic | GRCh37 (hg19) | NC_000013.10 | Chr13 | 87,918,047 | 87,918,047 | + | ||
| nssv18792375 | Submitted genomic | GRCh37 (hg19) | NC_000013.10 | Chr13 | 87,918,061 | 87,918,061 | - | ||
| nssv18792367 | Submitted genomic | GRCh37 (hg19) | NC_000013.10 | Chr13 | 107,614,717 | 107,614,717 | - | ||
| nssv18792376 | Submitted genomic | GRCh37 (hg19) | NC_000013.10 | Chr13 | 107,614,717 | 107,614,717 | + | ||
| nssv18792376 | Submitted genomic | GRCh37 (hg19) | NC_000013.10 | Chr13 | 107,657,183 | 107,657,183 | - | ||
| nssv18792366 | Submitted genomic | GRCh37 (hg19) | NC_000013.10 | Chr13 | 107,657,185 | 107,657,185 | + | ||
| nssv18792378 | Submitted genomic | GRCh37 (hg19) | NC_000015.9 | Chr15 | 98,510,600 | 98,510,600 | + | ||
| nssv18792377 | Submitted genomic | GRCh37 (hg19) | NC_000015.9 | Chr15 | 98,510,601 | 98,510,601 | - | ||
| nssv18792371 | Submitted genomic | GRCh37 (hg19) | NC_000016.9 | Chr16 | 26,210,170 | 26,210,170 | - | ||
| nssv18792372 | Submitted genomic | GRCh37 (hg19) | NC_000016.9 | Chr16 | 26,210,189 | 26,210,189 | + |