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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd153 | nssv14252580 | copy number loss | Merging | Merging | No | 147.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 86287188 | 86848477 | Submitted genomic | |||||||||
| nstd153 | nssv14252580 | copy number loss | Merging | Merging | No | 147.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 86287188 | 86848477 | Submitted genomic | |||||||||
| nstd153 | nssv14252580 | copy number loss | Merging | Merging | No | 147.30 | GRCh38.p12 | NC_000016.10 | 16 | 86253582 | 86814871 | Remapped | 1 | ||||||||
| nstd153 | nssv14252581 | copy number loss | Merging | Merging | No | 158.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 86284317 | 87137746 | Submitted genomic | |||||||||
| nstd153 | nssv14252581 | copy number loss | Merging | Merging | No | 158.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 86284317 | 87137746 | Submitted genomic | |||||||||
| nstd153 | nssv14252581 | copy number loss | Merging | Merging | No | 158.30 | GRCh38.p12 | NC_000016.10 | 16 | 86250711 | 87104140 | Remapped | 1 | ||||||||
| nstd153 | nssv14252582 | copy number loss | Merging | Merging | No | 54.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 85910504 | 86271710 | Submitted genomic | |||||||||
| nstd153 | nssv14252582 | copy number loss | Merging | Merging | No | 54.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 85910504 | 86271710 | Submitted genomic | |||||||||
| nstd153 | nssv14252582 | copy number loss | Merging | Merging | No | 54.30 | GRCh38.p12 | NC_000016.10 | 16 | 85876898 | 86238104 | Remapped | 1 | ||||||||
| nstd153 | nssv14252583 | copy number loss | Merging | Merging | No | 153.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 86208967 | 86301397 | Submitted genomic | |||||||||
| nstd153 | nssv14252583 | copy number loss | Merging | Merging | No | 153.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 86208967 | 86301397 | Submitted genomic | |||||||||
| nstd153 | nssv14252583 | copy number loss | Merging | Merging | No | 153.30 | GRCh38.p12 | NC_000016.10 | 16 | 86175361 | 86267791 | Remapped | 1 | ||||||||
| nstd153 | nssv14252584 | copy number loss | Merging | Merging | No | 155.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 84491194 | 86272042 | Submitted genomic | |||||||||
| nstd153 | nssv14252584 | copy number loss | Merging | Merging | No | 155.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 84491194 | 86272042 | Submitted genomic | |||||||||
| nstd153 | nssv14252584 | copy number loss | Merging | Merging | No | 155.30 | GRCh38.p12 | NC_000016.10 | 16 | 84457588 | 86238436 | Remapped | 1 | ||||||||
| nstd153 | nssv14252585 | copy number loss | Merging | Merging | No | 165.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 83672829 | 86268910 | Submitted genomic | |||||||||
| nstd153 | nssv14252585 | copy number loss | Merging | Merging | No | 165.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 83672829 | 86268910 | Submitted genomic | |||||||||
| nstd153 | nssv14252585 | copy number loss | Merging | Merging | No | 165.30 | GRCh38.p12 | NC_000016.10 | 16 | 83639224 | 86235304 | Remapped | 1 | ||||||||
| nstd153 | nssv14252586 | copy number loss | Merging | Merging | No | 177.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 82174710 | 86268909 | Submitted genomic | |||||||||
| nstd153 | nssv14252586 | copy number loss | Merging | Merging | No | 177.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 82174710 | 86268909 | Submitted genomic | |||||||||
| nstd153 | nssv14252586 | copy number loss | Merging | Merging | No | 177.30 | GRCh38.p12 | NC_000016.10 | 16 | 82141105 | 86235303 | Remapped | 1 | ||||||||
| nstd153 | nssv14252587 | copy number loss | Merging | Merging | No | 179.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 83671523 | 86296478 | Submitted genomic | |||||||||
| nstd153 | nssv14252587 | copy number loss | Merging | Merging | No | 179.30 | GRCh37 (hg19) | NC_000016.9 | 16 | 83671523 | 86296478 | Submitted genomic | |||||||||
| nstd153 | nssv14252587 | copy number loss | Merging | Merging | No | 179.30 | GRCh38.p12 | NC_000016.10 | 16 | 83637918 | 86262872 | Remapped | 1 |