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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd204 | nssv16788224 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 78958 | 81445 | Submitted genomic | |||||||||
| nstd204 | nssv16788281 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 85136 | 86644 | Submitted genomic | |||||||||
| nstd204 | nssv16788302 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 86645 | 91390 | Submitted genomic | |||||||||
| nstd204 | nssv16789323 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 55111 | 56781 | Submitted genomic | |||||||||
| nstd204 | nssv16789378 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 61382 | 62950 | Submitted genomic | |||||||||
| nstd204 | nssv16816932 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 91001 | 91800 | Submitted genomic | |||||||||
| nstd204 | nssv16817196 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 60101 | 61900 | Submitted genomic | |||||||||
| nstd204 | nssv16817753 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 79101 | 82000 | Submitted genomic | |||||||||
| nstd204 | nssv16817805 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 92401 | 93300 | Submitted genomic | |||||||||
| nstd204 | nssv16818149 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 39901 | 64200 | Submitted genomic | |||||||||
| nstd204 | nssv16818322 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 86601 | 90300 | Submitted genomic | |||||||||
| nstd204 | nssv16818465 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 76801 | 92000 | Submitted genomic | |||||||||
| nstd204 | nssv16818586 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 60101 | 60900 | Submitted genomic | |||||||||
| nstd204 | nssv16818647 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 11601 | 15700 | Submitted genomic | |||||||||
| nstd204 | nssv16818742 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 22801 | 26900 | Submitted genomic | |||||||||
| nstd204 | nssv16818993 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 61601 | 63000 | Submitted genomic | |||||||||
| nstd204 | nssv16819354 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 24301 | 128700 | Submitted genomic | |||||||||
| nstd204 | nssv16819571 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 75601 | 92900 | Submitted genomic | |||||||||
| nstd204 | nssv16819616 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 61201 | 63900 | Submitted genomic | |||||||||
| nstd204 | nssv16819704 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 68801 | 80600 | Submitted genomic | |||||||||
| nstd204 | nssv16819994 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 51401 | 52300 | Submitted genomic | |||||||||
| nstd204 | nssv16820181 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 70101 | 70900 | Submitted genomic | |||||||||
| nstd204 | nssv16820721 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 61501 | 68800 | Submitted genomic | |||||||||
| nstd204 | nssv16820861 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 44601 | 46200 | Submitted genomic | |||||||||
| nstd204 | nssv16820912 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 86501 | 95100 | Submitted genomic | |||||||||
| nstd204 | nssv16821004 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 12701 | 13400 | Submitted genomic | |||||||||
| nstd204 | nssv16821034 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 77601 | 86900 | Submitted genomic | |||||||||
| nstd204 | nssv16821295 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 66701 | 139900 | Submitted genomic | |||||||||
| nstd204 | nssv16821339 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 91701 | 125000 | Submitted genomic | |||||||||
| nstd204 | nssv16821361 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 52601 | 53300 | Submitted genomic | |||||||||
| nstd204 | nssv16821495 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 44701 | 58300 | Submitted genomic | |||||||||
| nstd204 | nssv16821587 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 24301 | 26900 | Submitted genomic | |||||||||
| nstd204 | nssv16821597 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 101901 | 102800 | Submitted genomic | |||||||||
| nstd204 | nssv16821761 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 15801 | 16100 | Submitted genomic | |||||||||
| nstd204 | nssv16822024 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 84901 | 86600 | Submitted genomic | |||||||||
| nstd204 | nssv16822044 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 56401 | 57000 | Submitted genomic | |||||||||
| nstd204 | nssv16822157 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 97401 | 97900 | Submitted genomic | |||||||||
| nstd204 | nssv16822284 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 58301 | 61200 | Submitted genomic | |||||||||
| nstd204 | nssv16822396 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 92701 | 114600 | Submitted genomic | |||||||||
| nstd204 | nssv16822546 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 91701 | 102300 | Submitted genomic | |||||||||
| nstd204 | nssv16822929 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 91901 | 119300 | Submitted genomic | |||||||||
| nstd204 | nssv16823258 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 98301 | 98700 | Submitted genomic | |||||||||
| nstd204 | nssv16823499 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 54001 | 56200 | Submitted genomic | |||||||||
| nstd204 | nssv16823578 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 49601 | 51400 | Submitted genomic | |||||||||
| nstd204 | nssv16823646 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 49601 | 57900 | Submitted genomic | |||||||||
| nstd204 | nssv16823723 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 60101 | 92000 | Submitted genomic | |||||||||
| nstd204 | nssv16823925 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 73701 | 74200 | Submitted genomic | |||||||||
| nstd204 | nssv16824242 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 82901 | 83400 | Submitted genomic | |||||||||
| nstd204 | nssv16824342 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 50601 | 54600 | Submitted genomic | |||||||||
| nstd204 | nssv16824453 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 16201 | 20700 | Submitted genomic | |||||||||
| nstd204 | nssv16824475 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 72701 | 92900 | Submitted genomic | |||||||||
| nstd204 | nssv16824686 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 47401 | 51200 | Submitted genomic | |||||||||
| nstd204 | nssv16824727 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 69701 | 72700 | Submitted genomic | |||||||||
| nstd204 | nssv16824871 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 24301 | 25700 | Submitted genomic | |||||||||
| nstd204 | nssv16824910 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 46601 | 47400 | Submitted genomic | |||||||||
| nstd204 | nssv16825382 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 78801 | 80200 | Submitted genomic | |||||||||
| nstd204 | nssv16825521 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 54001 | 54700 | Submitted genomic | |||||||||
| nstd204 | nssv16825898 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 11601 | 20700 | Submitted genomic | |||||||||
| nstd204 | nssv16825993 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 47401 | 53700 | Submitted genomic | |||||||||
| nstd204 | nssv16826298 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 69401 | 78900 | Submitted genomic | |||||||||
| nstd204 | nssv16826524 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 51301 | 53300 | Submitted genomic | |||||||||
| nstd204 | nssv16826634 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 56401 | 58300 | Submitted genomic | |||||||||
| nstd204 | nssv16826816 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 65901 | 69700 | Submitted genomic | |||||||||
| nstd204 | nssv16826861 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 71901 | 102800 | Submitted genomic | |||||||||
| nstd204 | nssv16827146 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 20701 | 95200 | Submitted genomic | |||||||||
| nstd204 | nssv16827559 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 75701 | 80500 | Submitted genomic | |||||||||
| nstd204 | nssv16827602 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 55101 | 56000 | Submitted genomic | |||||||||
| nstd204 | nssv16827887 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 89201 | 91900 | Submitted genomic | |||||||||
| nstd204 | nssv16828437 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 95001 | 98300 | Submitted genomic | |||||||||
| nstd204 | nssv16828502 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 63001 | 64200 | Submitted genomic | |||||||||
| nstd204 | nssv16828573 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 58301 | 59600 | Submitted genomic | |||||||||
| nstd204 | nssv16829126 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 77001 | 77600 | Submitted genomic | |||||||||
| nstd204 | nssv16829261 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 93301 | 96500 | Submitted genomic | |||||||||
| nstd204 | nssv16829384 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 49201 | 49600 | Submitted genomic | |||||||||
| nstd204 | nssv16829604 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 65901 | 106900 | Submitted genomic | |||||||||
| nstd204 | nssv16829648 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 60001 | 83500 | Submitted genomic | |||||||||
| nstd204 | nssv16830691 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 75701 | 78300 | Submitted genomic | |||||||||
| nstd204 | nssv16830848 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 71901 | 78300 | Submitted genomic | |||||||||
| nstd204 | nssv16831031 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 44601 | 47400 | Submitted genomic | |||||||||
| nstd204 | nssv16831435 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 68801 | 70900 | Submitted genomic | |||||||||
| nstd204 | nssv16831540 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 82001 | 83200 | Submitted genomic | |||||||||
| nstd204 | nssv16831598 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 74601 | 75100 | Submitted genomic | |||||||||
| nstd204 | nssv16831657 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 99101 | 102800 | Submitted genomic | |||||||||
| nstd204 | nssv16831687 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 100601 | 102800 | Submitted genomic | |||||||||
| nstd204 | nssv16832529 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 90701 | 93400 | Submitted genomic | |||||||||
| nstd204 | nssv16832533 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 71901 | 74200 | Submitted genomic | |||||||||
| nstd204 | nssv16832555 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 45701 | 48500 | Submitted genomic | |||||||||
| nstd204 | nssv16832711 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 99601 | 99800 | Submitted genomic | |||||||||
| nstd204 | nssv16833615 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 36301 | 37200 | Submitted genomic | |||||||||
| nstd204 | nssv16833916 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 51401 | 71200 | Submitted genomic | |||||||||
| nstd204 | nssv16833979 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 55101 | 58300 | Submitted genomic | |||||||||
| nstd204 | nssv16834051 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 101901 | 107400 | Submitted genomic | |||||||||
| nstd204 | nssv16834182 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 84101 | 90300 | Submitted genomic | |||||||||
| nstd204 | nssv16834691 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 97201 | 99000 | Submitted genomic | |||||||||
| nstd204 | nssv16834728 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 55101 | 57000 | Submitted genomic | |||||||||
| nstd204 | nssv16835023 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 61201 | 61600 | Submitted genomic | |||||||||
| nstd204 | nssv16835692 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 60101 | 67700 | Submitted genomic | |||||||||
| nstd204 | nssv16835948 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 75701 | 76400 | Submitted genomic | |||||||||
| nstd204 | nssv16835959 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 67101 | 67800 | Submitted genomic | |||||||||
| nstd204 | nssv16836352 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 68801 | 74200 | Submitted genomic |