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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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| nstd162 | nsv3319178 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 12501 | 12601 | 12701 | 27000 | 27100 | 27200 | Submitted genomic | ||||||||
| nstd162 | nsv3319178 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 12501 | 12601 | 12701 | 27000 | 27100 | 27200 | Submitted genomic | ||||||||
| nstd162 | nsv3319209 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 136212 | 136308 | Submitted genomic | ||||||||||||
| nstd162 | nsv3319209 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 136212 | 136308 | Submitted genomic | ||||||||||||
| nstd162 | nsv3319231 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 101701 | 101801 | 101901 | 126300 | 126400 | 126500 | Submitted genomic | ||||||||
| nstd162 | nsv3319231 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 101701 | 101801 | 101901 | 126300 | 126400 | 126500 | Submitted genomic | ||||||||
| nstd162 | nsv3319479 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 10401 | 10501 | 10601 | 78100 | 78200 | 78300 | Submitted genomic | ||||||||
| nstd162 | nsv3319479 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 10401 | 10501 | 10601 | 78100 | 78200 | 78300 | Submitted genomic | ||||||||
| nstd162 | nsv3319646 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 136935 | 136935 | Submitted genomic | ||||||||||||
| nstd162 | nsv3319646 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 136935 | 136935 | Submitted genomic | ||||||||||||
| nstd162 | nsv3319854 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 136935 | 136935 | Submitted genomic | ||||||||||||
| nstd162 | nsv3319854 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 136935 | 136935 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320775 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180094 | 180094 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320775 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180094 | 180094 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320776 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180097 | 180152 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320776 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180097 | 180152 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320777 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180345 | 180427 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320777 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180345 | 180427 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320779 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180750 | 180910 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320779 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180750 | 180910 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320784 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 181264 | 181264 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320784 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 181264 | 181264 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320970 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180170 | 180170 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320970 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180170 | 180170 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320971 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180209 | 180608 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320971 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180209 | 180608 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320972 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180201 | 180301 | 180401 | 194400 | 194500 | 194600 | Submitted genomic | ||||||||
| nstd162 | nsv3320972 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180201 | 180301 | 180401 | 194400 | 194500 | 194600 | Submitted genomic | ||||||||
| nstd162 | nsv3320976 | mobile element insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180529 | 180529 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320976 | mobile element insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180529 | 180529 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320981 | mobile element deletion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 181361 | 181482 | Submitted genomic | ||||||||||||
| nstd162 | nsv3320981 | mobile element deletion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 181361 | 181482 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321203 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180520 | 180694 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321203 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180520 | 180694 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321206 | mobile element insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180792 | 180792 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321206 | mobile element insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180792 | 180792 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321207 | mobile element insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180875 | 180875 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321207 | mobile element insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180875 | 180875 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321209 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180918 | 180991 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321209 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180918 | 180991 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321210 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180986 | 180986 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321210 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180986 | 180986 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321214 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 181153 | 181278 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321214 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 181153 | 181278 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321215 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 181211 | 181449 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321215 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 181211 | 181449 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321266 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 189845 | 189913 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321266 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 189845 | 189913 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321393 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180202 | 180202 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321393 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180202 | 180202 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321395 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180236 | 180367 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321395 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180236 | 180367 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321397 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180374 | 180505 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321397 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 180374 | 180505 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321449 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 191371 | 191371 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321449 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 191371 | 191371 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321987 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 204558 | 204558 | Submitted genomic | ||||||||||||
| nstd162 | nsv3321987 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 204558 | 204558 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323225 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 257803 | 257803 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323225 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 257803 | 257803 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323425 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 257995 | 257995 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323425 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 257995 | 257995 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323526 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 273189 | 275267 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323526 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 273189 | 275267 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323745 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 266201 | 266301 | 266401 | 290300 | 290400 | 290500 | Submitted genomic | ||||||||
| nstd162 | nsv3323745 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 266201 | 266301 | 266401 | 290300 | 290400 | 290500 | Submitted genomic | ||||||||
| nstd162 | nsv3323890 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 369927 | 369927 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323890 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 369927 | 369927 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323893 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 372682 | 372733 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323893 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 372682 | 372733 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323901 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 381171 | 381171 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323901 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 381171 | 381171 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323902 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 382318 | 382420 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323902 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 382318 | 382420 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323944 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 433889 | 433889 | Submitted genomic | ||||||||||||
| nstd162 | nsv3323944 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 433889 | 433889 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324027 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 596631 | 596732 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324027 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 596631 | 596732 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324028 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 597783 | 597783 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324028 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 597783 | 597783 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324042 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 60801 | 60901 | 61001 | 71400 | 71500 | 71600 | Submitted genomic | ||||||||
| nstd162 | nsv3324042 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 60801 | 60901 | 61001 | 71400 | 71500 | 71600 | Submitted genomic | ||||||||
| nstd162 | nsv3324043 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 610250 | 610250 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324043 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 610250 | 610250 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324044 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 611896 | 611896 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324044 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 611896 | 611896 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324117 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 257716 | 257716 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324117 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 257716 | 257716 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324123 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 264159 | 265579 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324123 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 264159 | 265579 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324320 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 369476 | 369616 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324320 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 369476 | 369616 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324321 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 369577 | 369577 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324321 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 369577 | 369577 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324324 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 370024 | 370024 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324324 | insertion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 370024 | 370024 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324325 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 372709 | 372760 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324325 | copy number variation | No | GRCh38 (hg38) | NC_000001.11 | 1 | 372709 | 372760 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324370 | mobile element deletion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 432590 | 432666 | Submitted genomic | ||||||||||||
| nstd162 | nsv3324370 | mobile element deletion | No | GRCh38 (hg38) | NC_000001.11 | 1 | 432590 | 432666 | Submitted genomic |