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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd221 | nssv17976487 | deletion | Sequencing | Sequence alignment | No | FXH | GRCh37.p13 | NC_000016.9 | 16 | 207988 | 289136 | Remapped | 1 | ||||||||
| nstd221 | nssv17976487 | deletion | Sequencing | Sequence alignment | No | FXH | GRCh37.p13 | NC_000016.9 | 16 | 207988 | 289136 | Remapped | 1 | ||||||||
| nstd221 | nssv17976487 | deletion | Sequencing | Sequence alignment | No | FXH | GRCh38 (hg38) | NC_000016.10 | 16 | 157989 | 239137 | Submitted genomic | |||||||||
| nstd221 | nssv17976487 | deletion | Sequencing | Sequence alignment | No | FXH | GRCh38 (hg38) | NC_000016.10 | 16 | 157989 | 239137 | Submitted genomic | |||||||||
| nstd221 | nssv17976488 | deletion | Sequencing | Sequence alignment | No | WYR | GRCh37.p13 | NC_000016.9 | 16 | 208664 | 235973 | Remapped | 1 | ||||||||
| nstd221 | nssv17976488 | deletion | Sequencing | Sequence alignment | No | WYR | GRCh37.p13 | NC_000016.9 | 16 | 208664 | 235973 | Remapped | 1 | ||||||||
| nstd221 | nssv17976488 | deletion | Sequencing | Sequence alignment | No | WYR | GRCh38 (hg38) | NC_000016.10 | 16 | 158665 | 185974 | Submitted genomic | |||||||||
| nstd221 | nssv17976488 | deletion | Sequencing | Sequence alignment | No | WYR | GRCh38 (hg38) | NC_000016.10 | 16 | 158665 | 185974 | Submitted genomic | |||||||||
| nstd221 | nssv17976489 | deletion | Sequencing | Sequence alignment | No | LYB | GRCh37.p13 | NC_000016.9 | 16 | 221251 | 266414 | Remapped | 1 | ||||||||
| nstd221 | nssv17976489 | deletion | Sequencing | Sequence alignment | No | LYB | GRCh37.p13 | NC_000016.9 | 16 | 221251 | 266414 | Remapped | 1 | ||||||||
| nstd221 | nssv17976489 | deletion | Sequencing | Sequence alignment | No | LYB | GRCh38 (hg38) | NC_000016.10 | 16 | 171252 | 216415 | Submitted genomic | |||||||||
| nstd221 | nssv17976489 | deletion | Sequencing | Sequence alignment | No | LYB | GRCh38 (hg38) | NC_000016.10 | 16 | 171252 | 216415 | Submitted genomic | |||||||||
| nstd221 | nssv17976490 | delins | Sequencing | Sequence alignment | No | WG | GRCh37.p13 | NC_000016.9 | 16 | 212933 | 236024 | Remapped | 1 | ||||||||
| nstd221 | nssv17976490 | delins | Sequencing | Sequence alignment | No | WG | GRCh37.p13 | NC_000016.9 | 16 | 212933 | 236024 | Remapped | 1 | ||||||||
| nstd221 | nssv17976490 | delins | Sequencing | Sequence alignment | No | WG | GRCh38 (hg38) | NC_000016.10 | 16 | 162934 | 186025 | Submitted genomic | |||||||||
| nstd221 | nssv17976490 | delins | Sequencing | Sequence alignment | No | WG | GRCh38 (hg38) | NC_000016.10 | 16 | 162934 | 186025 | Submitted genomic |