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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd166 | nssv15780791 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 46000 | 111250 | Remapped | 1 | ||||||||
| nstd166 | nssv15780792 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 46000 | 111250 | Remapped | 1 | ||||||||
| nstd166 | nssv15780793 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 46000 | 111250 | Remapped | 1 | ||||||||
| nstd166 | nssv15780794 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 46000 | 111250 | Remapped | 1 | ||||||||
| nstd166 | nssv15780795 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 46000 | 111250 | Remapped | 1 | ||||||||
| nstd166 | nssv15780796 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 46000 | 111250 | Remapped | 1 | ||||||||
| nstd166 | nssv15780797 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 46000 | 111250 | Remapped | 1 | ||||||||
| nstd166 | nssv15780798 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 46000 | 111250 | Remapped | 1 | ||||||||
| nstd166 | nssv15780799 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 46000 | 111250 | Remapped | 1 | ||||||||
| nstd166 | nssv15780869 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 94000 | 129400 | Remapped | 1 | ||||||||
| nstd166 | nssv15780870 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 94000 | 129400 | Remapped | 1 | ||||||||
| nstd166 | nssv15780871 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 94000 | 129400 | Remapped | 1 | ||||||||
| nstd166 | nssv15780872 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 94000 | 129400 | Remapped | 1 | ||||||||
| nstd166 | nssv15780873 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 94000 | 129400 | Remapped | 1 | ||||||||
| nstd166 | nssv15780874 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 94000 | 129400 | Remapped | 1 | ||||||||
| nstd166 | nssv15780875 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 94000 | 129400 | Remapped | 1 | ||||||||
| nstd166 | nssv15780935 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 123350 | 140100 | Remapped | 1 | ||||||||
| nstd166 | nssv15780936 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 123350 | 140100 | Remapped | 1 | ||||||||
| nstd166 | nssv15780937 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 123350 | 140100 | Remapped | 1 | ||||||||
| nstd166 | nssv15780938 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 123350 | 140100 | Remapped | 1 | ||||||||
| nstd166 | nssv15780939 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 123350 | 140100 | Remapped | 1 | ||||||||
| nstd166 | nssv15780940 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 123350 | 140100 | Remapped | 1 | ||||||||
| nstd166 | nssv15780941 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 123350 | 140100 | Remapped | 1 | ||||||||
| nstd166 | nssv15781041 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 257999 | 289549 | Remapped | 1 | ||||||||
| nstd166 | nssv15781042 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 257999 | 289549 | Remapped | 1 | ||||||||
| nstd166 | nssv15781043 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 257999 | 289549 | Remapped | 1 | ||||||||
| nstd166 | nssv15781044 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 257999 | 289549 | Remapped | 1 | ||||||||
| nstd166 | nssv15781045 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 257999 | 289549 | Remapped | 1 | ||||||||
| nstd166 | nssv15781046 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 257999 | 289549 | Remapped | 1 | ||||||||
| nstd166 | nssv15781047 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 257999 | 289549 | Remapped | 1 | ||||||||
| nstd166 | nssv15781048 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 257999 | 289549 | Remapped | 1 | ||||||||
| nstd166 | nssv15781114 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 431337 | 436337 | Remapped | 1 | ||||||||
| nstd166 | nssv15781115 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 431337 | 436337 | Remapped | 1 | ||||||||
| nstd166 | nssv15781116 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 431337 | 436337 | Remapped | 1 | ||||||||
| nstd166 | nssv15781117 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 431337 | 436337 | Remapped | 1 | ||||||||
| nstd166 | nssv15781118 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 431337 | 436337 | Remapped | 1 | ||||||||
| nstd166 | nssv15781119 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 431337 | 436337 | Remapped | 1 | ||||||||
| nstd166 | nssv15781120 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 431337 | 436337 | Remapped | 1 | ||||||||
| nstd166 | nssv15781121 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 431337 | 436337 | Remapped | 1 | ||||||||
| nstd166 | nssv15781122 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 431337 | 436337 | Remapped | 1 | ||||||||
| nstd166 | nssv15781123 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 431337 | 436337 | Remapped | 1 | ||||||||
| nstd166 | nssv15781124 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 431337 | 436337 | Remapped | 1 | ||||||||
| nstd166 | nssv15781125 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 431337 | 436337 | Remapped | 1 | ||||||||
| nstd166 | nssv15781229 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 586420 | 611470 | Remapped | 1 | ||||||||
| nstd166 | nssv15781230 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 586420 | 611470 | Remapped | 1 | ||||||||
| nstd166 | nssv15781231 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 586420 | 611470 | Remapped | 1 | ||||||||
| nstd166 | nssv15781232 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 586420 | 611470 | Remapped | 1 | ||||||||
| nstd166 | nssv15781233 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 586420 | 611470 | Remapped | 1 | ||||||||
| nstd166 | nssv15781234 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 586420 | 611470 | Remapped | 1 | ||||||||
| nstd166 | nssv15781235 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 586420 | 611470 | Remapped | 1 | ||||||||
| nstd166 | nssv15781236 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 586420 | 611470 | Remapped | 1 | ||||||||
| nstd166 | nssv15781319 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 617920 | 629020 | Remapped | 1 | ||||||||
| nstd166 | nssv15781320 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 617920 | 629020 | Remapped | 1 | ||||||||
| nstd166 | nssv15781321 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 617920 | 629020 | Remapped | 1 | ||||||||
| nstd166 | nssv15781322 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 617920 | 629020 | Remapped | 1 | ||||||||
| nstd166 | nssv15781323 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 617920 | 629020 | Remapped | 1 | ||||||||
| nstd166 | nssv15781324 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 617920 | 629020 | Remapped | 1 | ||||||||
| nstd166 | nssv15781325 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 617920 | 629020 | Remapped | 1 | ||||||||
| nstd166 | nssv15781424 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781425 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781426 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781427 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781428 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781429 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781430 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781431 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781432 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781433 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781434 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781435 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781436 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781437 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15781438 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15783355 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15783356 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15783357 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15783358 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15783359 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15783360 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 624870 | 635220 | Remapped | 1 | ||||||||
| nstd166 | nssv15783384 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 663920 | 669870 | Remapped | 1 | ||||||||
| nstd166 | nssv15783385 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 663920 | 669870 | Remapped | 1 | ||||||||
| nstd166 | nssv15783386 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 663920 | 669870 | Remapped | 1 | ||||||||
| nstd166 | nssv15783387 | copy number variation | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 663920 | 669870 | Remapped | 1 | ||||||||
| nstd166 | nssv15845703 | deletion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 460337 | 465337 | Remapped | 1 | ||||||||
| nstd166 | nssv15847505 | deletion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 417587 | 455337 | Remapped | 1 | ||||||||
| nstd166 | nssv15850204 | deletion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 636370 | 649645 | Remapped | 1 | ||||||||
| nstd166 | nssv15850344 | deletion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 595720 | 678370 | Remapped | 1 | ||||||||
| nstd166 | nssv15851040 | deletion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 639370 | 646570 | Remapped | 1 | ||||||||
| nstd166 | nssv15851241 | deletion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 62399 | 62489 | Remapped | 1 | ||||||||
| nstd166 | nssv15853163 | deletion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 66350 | 66427 | Remapped | 1 | ||||||||
| nstd166 | nssv15855340 | deletion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 274165 | 274481 | Remapped | 1 | ||||||||
| nstd166 | nssv15856828 | deletion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 491687 | 499337 | Remapped | 1 | ||||||||
| nstd166 | nssv15964044 | duplication | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 137000 | 155500 | Remapped | 1 | ||||||||
| nstd166 | nssv15965142 | duplication | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 612219 | 612422 | Remapped | 1 | ||||||||
| nstd166 | nssv15965365 | duplication | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 141475 | 155000 | Remapped | 1 | ||||||||
| nstd166 | nssv16023685 | insertion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 66531 | 66531 | Remapped | 1 | ||||||||
| nstd166 | nssv16024555 | insertion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 54665 | 54665 | Remapped | 1 | ||||||||
| nstd166 | nssv16025254 | insertion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 66576 | 66576 | Remapped | 1 | ||||||||
| nstd166 | nssv16026934 | insertion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 79210 | 79210 | Remapped | 1 | ||||||||
| nstd166 | nssv16029986 | insertion | 1 | Sequencing | Other | No | GRCh38.p12 | NC_000001.11 | 1 | 595506 | 595506 | Remapped | 1 |