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| Study ID | Variant ID | Variant Region type | Variant Call type | Sampleset ID | Method | Analysis ID | Validation | Variant samples | Subject phenotype | Clinical Interpretation | Assembly | Accession | Chr | Outer-Start | Start | Inner-Start | Inner-End | End | Outer-End | Placement Type | Remap Score |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd163 | nsv3318981 | copy number variation | No | GRCh37 (hg19) | NC_000018.9 | 18 | 109019 | 109155 | Submitted genomic | ||||||||||||
| nstd163 | nsv3318981 | copy number variation | No | GRCh37 (hg19) | NC_000018.9 | 18 | 109019 | 109155 | Submitted genomic | ||||||||||||
| nstd163 | nsv3318981 | copy number variation | No | GRCh38.p12 | NC_000018.10 | 18 | 109019 | 109155 | Remapped | 1 | |||||||||||
| nstd163 | nsv3318982 | copy number variation | No | GRCh37 (hg19) | NC_000020.10 | 20 | 25834741 | 25834820 | Submitted genomic | ||||||||||||
| nstd163 | nsv3318982 | copy number variation | No | GRCh37 (hg19) | NC_000020.10 | 20 | 25834741 | 25834820 | Submitted genomic | ||||||||||||
| nstd163 | nsv3318982 | copy number variation | No | GRCh38.p12 | NC_000020.11 | 20 | 25854105 | 25854184 | Remapped | 1 | |||||||||||
| nstd163 | nsv3318983 | copy number variation | No | GRCh37 (hg19) | NC_000006.11 | 6 | 168476538 | 168476599 | Submitted genomic | ||||||||||||
| nstd163 | nsv3318983 | copy number variation | No | GRCh37 (hg19) | NC_000006.11 | 6 | 168476538 | 168476599 | Submitted genomic | ||||||||||||
| nstd163 | nsv3318983 | copy number variation | No | GRCh38.p12 | NC_000006.12 | 6 | 168075858 | 168075919 | Remapped | 1 |