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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd164 | nsv3418821 | copy number variation | No | GRCh37 (hg19) | NC_000005.9 | 5 | 43957152 | 43957220 | 46135141 | 46135209 | Submitted genomic | ||||||||||
| nstd164 | nsv3418821 | copy number variation | No | GRCh37 (hg19) | NC_000005.9 | 5 | 43957152 | 43957220 | 46135141 | 46135209 | Submitted genomic | ||||||||||
| nstd164 | nsv3418821 | copy number variation | No | GRCh38.p12 | NC_000005.10 | 5 | 43957050 | 43957118 | 46135039 | 46135107 | Remapped | 1 | |||||||||
| nstd164 | nsv3418822 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 58088933 | 58089453 | 60345508 | 60346028 | Submitted genomic | ||||||||||
| nstd164 | nsv3418822 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 58088933 | 58089453 | 60345508 | 60346028 | Submitted genomic | ||||||||||
| nstd164 | nsv3418822 | copy number variation | No | GRCh38.p12 | NC_000017.11 | 17 | 60011572 | 60012092 | 62268147 | 62268667 | Remapped | 1 | |||||||||
| nstd164 | nsv3418823 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 59542891 | 59542894 | 59551500 | 59551503 | Submitted genomic | ||||||||||
| nstd164 | nsv3418823 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 59542891 | 59542894 | 59551500 | 59551503 | Submitted genomic | ||||||||||
| nstd164 | nsv3418823 | copy number variation | No | GRCh38.p12 | NC_000017.11 | 17 | 61465530 | 61465533 | 61474139 | 61474142 | Remapped | 1 | |||||||||
| nstd164 | nsv3418824 | copy number variation | No | GRCh37 (hg19) | NC_000005.9 | 5 | 42985023 | 45244787 | Submitted genomic | ||||||||||||
| nstd164 | nsv3418824 | copy number variation | No | GRCh37 (hg19) | NC_000005.9 | 5 | 42985023 | 45244787 | Submitted genomic | ||||||||||||
| nstd164 | nsv3418824 | copy number variation | No | GRCh38.p12 | NC_000005.10 | 5 | 42984921 | 45244685 | Remapped | 1 | |||||||||||
| nstd164 | nsv3418825 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 58167485 | 60174066 | Submitted genomic | ||||||||||||
| nstd164 | nsv3418825 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 58167485 | 60174066 | Submitted genomic | ||||||||||||
| nstd164 | nsv3418825 | copy number variation | No | GRCh38.p12 | NC_000017.11 | 17 | 60090124 | 62096705 | Remapped | 1 | |||||||||||
| nstd164 | nsv3418826 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 58086876 | 58087936 | 60343456 | 60344516 | Submitted genomic | ||||||||||
| nstd164 | nsv3418826 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 58086876 | 58087936 | 60343456 | 60344516 | Submitted genomic | ||||||||||
| nstd164 | nsv3418826 | copy number variation | No | GRCh38.p12 | NC_000017.11 | 17 | 60009515 | 60010575 | 62266095 | 62267155 | Remapped | 1 | |||||||||
| nstd164 | nsv3418827 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 58089454 | 58090137 | 60346028 | 60346711 | Submitted genomic | ||||||||||
| nstd164 | nsv3418827 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 58089454 | 58090137 | 60346028 | 60346711 | Submitted genomic | ||||||||||
| nstd164 | nsv3418827 | copy number variation | No | GRCh38.p12 | NC_000017.11 | 17 | 60012093 | 60012776 | 62268667 | 62269350 | Remapped | 1 | |||||||||
| nstd164 | nsv3418828 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 58090283 | 58090656 | 60346857 | 60347230 | Submitted genomic | ||||||||||
| nstd164 | nsv3418828 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 58090283 | 58090656 | 60346857 | 60347230 | Submitted genomic | ||||||||||
| nstd164 | nsv3418828 | copy number variation | No | GRCh38.p12 | NC_000017.11 | 17 | 60012922 | 60013295 | 62269496 | 62269869 | Remapped | 1 | |||||||||
| nstd164 | nsv3418829 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 58857889 | 58857898 | 58868328 | 58868337 | Submitted genomic | ||||||||||
| nstd164 | nsv3418829 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 58857889 | 58857898 | 58868328 | 58868337 | Submitted genomic | ||||||||||
| nstd164 | nsv3418829 | copy number variation | No | GRCh38.p12 | NC_000017.11 | 17 | 60780528 | 60780537 | 60790967 | 60790976 | Remapped | 1 | |||||||||
| nstd164 | nsv3418830 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 59272842 | 59272846 | 61392993 | 61392997 | Submitted genomic | ||||||||||
| nstd164 | nsv3418830 | copy number variation | No | GRCh37 (hg19) | NC_000017.10 | 17 | 59272842 | 59272846 | 61392993 | 61392997 | Submitted genomic | ||||||||||
| nstd164 | nsv3418830 | copy number variation | No | GRCh38.p12 | NC_000017.11 | 17 | 61195481 | 61195485 | 63315632 | 63315636 | Remapped | 1 |