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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970861insertion1nstd209human GRCh38 chr17: 72,073,402-72,073,402 , GRCh37.p13 chr17: 70,069,543-70,069,543 SOX9-AS1, LINC02097
    nsv5935632copy number variation1nstd209human GRCh38 chr17: 72,087,358-72,087,465 , GRCh37.p13 chr17: 70,083,499-70,083,606 LINC02097, SOX9-AS1
    nsv5710761mobile element insertion2nstd211human GRCh38 chr17: 72,073,413-72,073,413 , GRCh37.p13 chr17: 70,069,554-70,069,554 SOX9-AS1, LINC02097
    nsv5662909insertion1nstd207human GRCh38 chr17: 72,087,384-72,087,384 , GRCh37.p13 chr17: 70,083,525-70,083,525 SOX9-AS1, LINC02097
    nsv5598499copy number variation1nstd207human GRCh38 chr17: 72,087,362-72,087,453 , GRCh37.p13 chr17: 70,083,503-70,083,594 SOX9-AS1, LINC02097
    nsv5421978mobile element insertion1nstd206human GRCh38 chr17: 72,073,413-72,073,464 , GRCh37.p13 chr17: 70,069,554-70,069,605 SOX9-AS1, LINC02097
    nsv5349641translocation1nstd200human GRCh38 chr17: 72,087,968-72,087,968 , GRCh38 chr17: 72,087,306-72,087,306 , GRCh37.p13 chr17: 70,084,109-70,084,109 , GRCh37.p13 chr17: 70,083,447-70,083,447 LINC02097, SOX9-AS1
    nsv5336118translocation1nstd200human GRCh37 chr17: 70,083,447-70,083,447 , GRCh37 chr17: 70,084,109-70,084,109 , GRCh38.p12 chr17: 72,087,968-72,087,968 , GRCh38.p12 chr17: 72,087,306-72,087,306 LINC02097, SOX9-AS1
    nsv5155730mobile element insertion1nstd203human GRCh38 chr17: 72,073,395-72,073,413 , GRCh37.p13 chr17: 70,069,536-70,069,554 LINC02097, SOX9-AS1
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv4733806copy number variation1nstd199human GRCh37 chr17: 70,083,503-70,083,593 , GRCh38.p12 chr17: 72,087,362-72,087,452 LINC02097, SOX9-AS1
    nsv4567180mobile element insertion1nstd166human GRCh37.p13 chr17: 70,070,449-70,070,449 , GRCh38.p12 chr17: 72,074,308-72,074,308 SOX9-AS1, LINC02097
    nsv4507585mobile element insertion1nstd166human GRCh37.p13 chr17: 70,069,536-70,069,536 , GRCh38.p12 chr17: 72,073,395-72,073,395 LINC02097, SOX9-AS1
    nsv4504510mobile element insertion1nstd166human GRCh37.p13 chr17: 70,068,740-70,068,740 , GRCh38.p12 chr17: 72,072,599-72,072,599 LINC02097, SOX9-AS1
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4438294copy number variation1nstd175human GRCh37 chr17: 70,083,503-70,083,595 , GRCh38.p12 chr17: 72,087,362-72,087,454 SOX9-AS1, LINC02097
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4260109copy number variation1nstd166human GRCh37.p13 chr17: 70,084,336-70,084,568 , GRCh38.p12 chr17: 72,088,195-72,088,427 SOX9-AS1, LINC02097
    nsv4258238copy number variation1nstd166human GRCh37.p13 chr17: 70,083,447-70,084,109 , GRCh38.p12 chr17: 72,087,306-72,087,968 SOX9-AS1, LINC02097
    nsv4257569copy number variation1nstd166human GRCh37.p13 chr17: 70,083,512-70,083,587 , GRCh38.p12 chr17: 72,087,371-72,087,446 LINC02097, SOX9-AS1
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