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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd142 | nsv3067120 | sequence alteration | No | GRCh37.p13 | NC_000001.10 | 1 | 161539995 | 161549133 | Remapped | 1 | |||||||||||
| nstd142 | nsv3067120 | sequence alteration | No | GRCh37.p13 | NC_000001.10 | 1 | 161539995 | 161549133 | Remapped | 1 | |||||||||||
| nstd142 | nsv3067120 | sequence alteration | No | GRCh38.p12 | NC_000001.11 | 1 | 161570205 | 161579343 | Remapped | 1 | |||||||||||
| nstd142 | nsv3067120 | sequence alteration | No | NCBI36 (hg18) | NC_000001.9 | 1 | 159806619 | 159815757 | Submitted genomic | ||||||||||||
| nstd142 | nsv3067121 | sequence alteration | No | GRCh37.p13 | NC_000001.10 | 1 | 161621837 | 161630947 | Remapped | 1 | |||||||||||
| nstd142 | nsv3067121 | sequence alteration | No | GRCh37.p13 | NC_000001.10 | 1 | 161621837 | 161630947 | Remapped | 1 | |||||||||||
| nstd142 | nsv3067121 | sequence alteration | No | GRCh38.p12 | NC_000001.11 | 1 | 161652047 | 161661157 | Remapped | 1 | |||||||||||
| nstd142 | nsv3067121 | sequence alteration | No | NCBI36 (hg18) | NC_000001.9 | 1 | 159888461 | 159897571 | Submitted genomic | ||||||||||||
| nstd142 | nsv3067122 | sequence alteration | No | GRCh37.p13 | NC_000001.10 | 1 | 161621773 | 161624212 | Remapped | 1 | |||||||||||
| nstd142 | nsv3067122 | sequence alteration | No | GRCh37.p13 | NC_000001.10 | 1 | 161621773 | 161624212 | Remapped | 1 | |||||||||||
| nstd142 | nsv3067122 | sequence alteration | No | GRCh38.p12 | NC_000001.11 | 1 | 161651983 | 161654422 | Remapped | 1 | |||||||||||
| nstd142 | nsv3067122 | sequence alteration | No | NCBI36 (hg18) | NC_000001.9 | 1 | 159888397 | 159890836 | Submitted genomic |