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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 | 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 | nssv16817196 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 60101 | 61900 | Submitted genomic | |||||||||
| nstd204 | nssv16818149 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 39901 | 64200 | 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 | nssv16819616 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 61201 | 63900 | Submitted genomic | |||||||||
| nstd204 | nssv16819994 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 51401 | 52300 | 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 | nssv16821004 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 12701 | 13400 | 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 | nssv16821761 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 15801 | 16100 | Submitted genomic | |||||||||
| nstd204 | nssv16822044 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 56401 | 57000 | Submitted genomic | |||||||||
| nstd204 | nssv16822284 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 58301 | 61200 | 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 | 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 | nssv16824686 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 47401 | 51200 | 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 | 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 | 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 | nssv16827146 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 20701 | 95200 | Submitted genomic | |||||||||
| nstd204 | nssv16827602 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 55101 | 56000 | 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 | 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 | nssv16831031 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 44601 | 47400 | Submitted genomic | |||||||||
| nstd204 | nssv16832555 | copy number variation | 1 | Sequencing | Read depth | No | GRCh38.p13 | NC_000001.11 | 1 | 45701 | 48500 | 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 | 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 | nsv5200535 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 46601 | 47400 | Submitted genomic | ||||||||||||
| nstd204 | nsv5201969 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 24301 | 25700 | Submitted genomic | ||||||||||||
| nstd204 | nsv5202041 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 44601 | 46200 | Submitted genomic | ||||||||||||
| nstd204 | nsv5202429 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 44701 | 58300 | Submitted genomic | ||||||||||||
| nstd204 | nsv5202792 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 49601 | 51400 | Submitted genomic | ||||||||||||
| nstd204 | nsv5202841 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 55101 | 56000 | Submitted genomic | ||||||||||||
| nstd204 | nsv5203498 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 51401 | 71200 | Submitted genomic | ||||||||||||
| nstd204 | nsv5203618 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 24301 | 26900 | Submitted genomic | ||||||||||||
| nstd204 | nsv5204014 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 51301 | 53300 | Submitted genomic | ||||||||||||
| nstd204 | nsv5204609 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 47401 | 51200 | Submitted genomic | ||||||||||||
| nstd204 | nsv5204963 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 60001 | 83500 | Submitted genomic | ||||||||||||
| nstd204 | nsv5205139 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 20701 | 95200 | Submitted genomic | ||||||||||||
| nstd204 | nsv5205240 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 15801 | 16100 | Submitted genomic | ||||||||||||
| nstd204 | nsv5205443 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 54001 | 56200 | Submitted genomic | ||||||||||||
| nstd204 | nsv5205492 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 60101 | 61900 | Submitted genomic | ||||||||||||
| nstd204 | nsv5206588 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 16201 | 20700 | Submitted genomic | ||||||||||||
| nstd204 | nsv5206922 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 60101 | 92000 | Submitted genomic | ||||||||||||
| nstd204 | nsv5207526 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 39901 | 64200 | Submitted genomic | ||||||||||||
| nstd204 | nsv5207672 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 61201 | 61600 | Submitted genomic | ||||||||||||
| nstd204 | nsv5207723 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 61601 | 63000 | Submitted genomic | ||||||||||||
| nstd204 | nsv5208412 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 55101 | 57000 | Submitted genomic | ||||||||||||
| nstd204 | nsv5208513 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 22801 | 26900 | Submitted genomic | ||||||||||||
| nstd204 | nsv5208668 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 58301 | 61200 | Submitted genomic | ||||||||||||
| nstd204 | nsv5208765 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 47401 | 53700 | Submitted genomic | ||||||||||||
| nstd204 | nsv5208791 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 36301 | 37200 | Submitted genomic | ||||||||||||
| nstd204 | nsv5208849 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 61201 | 63900 | Submitted genomic | ||||||||||||
| nstd204 | nsv5210027 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 12701 | 13400 | Submitted genomic | ||||||||||||
| nstd204 | nsv5210058 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 54001 | 54700 | Submitted genomic | ||||||||||||
| nstd204 | nsv5210284 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 65901 | 69700 | Submitted genomic | ||||||||||||
| nstd204 | nsv5210487 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 56401 | 57000 | Submitted genomic | ||||||||||||
| nstd204 | nsv5210839 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 55101 | 58300 | Submitted genomic | ||||||||||||
| nstd204 | nsv5211180 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 60101 | 67700 | Submitted genomic | ||||||||||||
| nstd204 | nsv5213016 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 51401 | 52300 | Submitted genomic | ||||||||||||
| nstd204 | nsv5213099 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 65901 | 106900 | Submitted genomic | ||||||||||||
| nstd204 | nsv5213190 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 60101 | 60900 | Submitted genomic | ||||||||||||
| nstd204 | nsv5213558 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 52601 | 53300 | Submitted genomic | ||||||||||||
| nstd204 | nsv5213767 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 24301 | 128700 | Submitted genomic | ||||||||||||
| nstd204 | nsv5214136 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 61382 | 62950 | Submitted genomic | ||||||||||||
| nstd204 | nsv5214618 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 56401 | 58300 | Submitted genomic | ||||||||||||
| nstd204 | nsv5214994 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 50601 | 54600 | Submitted genomic | ||||||||||||
| nstd204 | nsv5215476 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 58301 | 59600 | Submitted genomic | ||||||||||||
| nstd204 | nsv5216203 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 55111 | 56781 | Submitted genomic | ||||||||||||
| nstd204 | nsv5216502 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 49201 | 49600 | Submitted genomic | ||||||||||||
| nstd204 | nsv5216604 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 49601 | 57900 | Submitted genomic | ||||||||||||
| nstd204 | nsv5217382 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 11601 | 20700 | Submitted genomic | ||||||||||||
| nstd204 | nsv5218481 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 44601 | 47400 | Submitted genomic | ||||||||||||
| nstd204 | nsv5218923 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 61501 | 68800 | Submitted genomic | ||||||||||||
| nstd204 | nsv5219332 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 45701 | 48500 | Submitted genomic | ||||||||||||
| nstd204 | nsv5219414 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 63001 | 64200 | Submitted genomic | ||||||||||||
| nstd204 | nsv5219885 | copy number variation | No | GRCh38.p13 | NC_000001.11 | 1 | 11601 | 15700 | Submitted genomic |