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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd182 | nsv4578341 | copy number variation | No | GRCh37 (hg19) | NC_000009.11 | 9 | 139252010 | 139435356 | Submitted genomic | ||||||||||||
| nstd182 | nsv4578341 | copy number variation | No | GRCh37 (hg19) | NC_000009.11 | 9 | 139252010 | 139435356 | Submitted genomic | ||||||||||||
| nstd182 | nsv4578341 | copy number variation | No | GRCh38.p12 | NC_000009.12 | 9 | 136357558 | 136540904 | Remapped | 1 | |||||||||||
| nstd182 | nsv4578342 | copy number variation | No | GRCh37 (hg19) | NC_000009.11 | 9 | 139375930 | 139435356 | Submitted genomic | ||||||||||||
| nstd182 | nsv4578342 | copy number variation | No | GRCh37 (hg19) | NC_000009.11 | 9 | 139375930 | 139435356 | Submitted genomic | ||||||||||||
| nstd182 | nsv4578342 | copy number variation | No | GRCh38.p12 | NC_000009.12 | 9 | 136481478 | 136540904 | Remapped | 1 | |||||||||||
| nstd182 | nsv4578343 | copy number variation | No | GRCh37 (hg19) | NC_000022.10 | 22 | 51073379 | 51197838 | Submitted genomic | ||||||||||||
| nstd182 | nsv4578343 | copy number variation | No | GRCh37 (hg19) | NC_000022.10 | 22 | 51073379 | 51197838 | Submitted genomic | ||||||||||||
| nstd182 | nsv4578343 | copy number variation | No | GRCh38.p12 | NC_000022.11 | 22 | 50634951 | 50759410 | Remapped | 1 | |||||||||||
| nstd182 | nsv4578343 | copy number variation | No | GRCh38.p12 | NW_015148969.1 | 22|NW_015148969.1 | 1 | 95522 | Remapped | 0.76749 | |||||||||||
| nstd182 | nsv4578344 | copy number variation | No | GRCh37 (hg19) | NC_000022.10 | 22 | 51127896 | 51197725 | Submitted genomic | ||||||||||||
| nstd182 | nsv4578344 | copy number variation | No | GRCh37 (hg19) | NC_000022.10 | 22 | 51127896 | 51197725 | Submitted genomic | ||||||||||||
| nstd182 | nsv4578344 | copy number variation | No | GRCh38.p12 | NC_000022.11 | 22 | 50689468 | 50759297 | Remapped | 1 | |||||||||||
| nstd182 | nsv4578344 | copy number variation | No | GRCh38.p12 | NW_015148969.1 | 22|NW_015148969.1 | 25379 | 95409 | Remapped | 1.00288 | |||||||||||
| nstd182 | nsv4578345 | copy number variation | No | GRCh37 (hg19) | NC_000014.8 | 14 | 79342954 | 79397500 | Submitted genomic | ||||||||||||
| nstd182 | nsv4578345 | copy number variation | No | GRCh37 (hg19) | NC_000014.8 | 14 | 79342954 | 79397500 | Submitted genomic | ||||||||||||
| nstd182 | nsv4578345 | copy number variation | No | GRCh38.p12 | NC_000014.9 | 14 | 78876611 | 78931157 | Remapped | 1 |