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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971191inversion1nstd209human GRCh37.p13 chr17: 21,250,948-21,517,390 , GRCh38 chr17: 21,330,941-21,766,277 , GRCh37.p13 chr17|NW_003315950.2: 1-418,641 KCNJ12, LINC02693, 6 more genes
    nsv5946794copy number variation1nstd209human GRCh38 chr17: 21,526,681-21,528,748 , GRCh37.p13 chr17: 21,429,942-21,432,009 , GRCh37.p13 chr17|NW_003315950.2: 179,046-181,113 LINC02693
    nsv5940845copy number variation1nstd209human GRCh37.p13 chr17|NW_003315950.2: 53,539-340,932 , GRCh38 chr17: 21,401,174-21,688,567 , GRCh37.p13 chr17: 21,304,486-21,517,390 KCNJ12, LINC02693, 5 more genes
    nsv5939520copy number variation1nstd209human GRCh37.p13 chr17: 21,323,049-21,517,390 , GRCh38 chr17: 21,419,737-21,705,634 , GRCh37.p13 chr17|NW_003315950.2: 72,102-357,999 KCNJ12, LINC02693, 6 more genes
    nsv5933440copy number variation1nstd209human GRCh37.p13 chr17|NW_003315950.2: 79,530-365,405 , GRCh38 chr17: 21,427,165-21,713,040 , GRCh37.p13 chr17: 21,330,477-21,517,390 LINC02693, RPL21P120, 5 more genes
    nsv5929137copy number variation1nstd209human GRCh37.p13 chr17|NW_003315950.2: 74,120-360,004 , GRCh38 chr17: 21,421,755-21,707,639 , GRCh37.p13 chr17: 21,325,067-21,517,390 LINC02693, RPL21P120, 5 more genes
    nsv5880414copy number variation2nstd209human GRCh38 chr17: 21,524,929-21,528,763 , GRCh37.p13 chr17|NW_003315950.2: 177,294-181,128 , GRCh37.p13 chr17: 21,428,190-21,432,024 LINC02693
    nsv5872132copy number variation1nstd209human GRCh38 chr17: 21,547,247-21,549,558 , GRCh37.p13 chr17|NW_003315950.2: 199,612-201,923 , GRCh37.p13 chr17: 21,450,510-21,452,821 LINC02693
    nsv5670902inversion1nstd207human GRCh37.p13 chr17: 19,143,942-21,250,947 , GRCh38 chr17: 19,240,629-21,558,840 , ALDH3A1, 86 more genes
    nsv5564104sequence alteration1nstd206human GRCh37.p13 chr17|NW_003315950.2: 174,595-644,425 , GRCh38 chr17: 21,522,230-22,444,234 , GRCh37.p13 chr17: 21,425,491-21,909,571 , KCNJ18, 15 more genes
    nsv5556888sequence alteration1nstd206human GRCh37.p13 chr17|NW_003315950.2: 1-432,162 , GRCh38 chr17: 21,308,158-21,779,798 , GRCh37.p13 chr17: 21,250,948-21,517,390 LOC100533653, LOC101930665, 8 more genes
    nsv5532118copy number variation1nstd206human GRCh38 chr17: 21,534,702-21,534,776 , GRCh37.p13 chr17|NW_003315950.2: 187,067-187,141 , GRCh37.p13 chr17: 21,437,963-21,438,037 LINC02693
    nsv5531612copy number variation1nstd206human GRCh37.p13 chr17|NW_003315950.2: 74,165-349,476 , GRCh38 chr17: 21,421,800-21,697,111 , GRCh37.p13 chr17: 21,325,112-21,517,390 LINC02693, RPL21P120, 5 more genes
    nsv5524619copy number variation1nstd206human GRCh38 chr17: 21,543,174-21,543,278 , GRCh37.p13 chr17|NW_003315950.2: 195,539-195,643 , GRCh37.p13 chr17: 21,446,437-21,446,541 LINC02693
    nsv5515751copy number variation1nstd206human GRCh37.p13 chr17|NW_003315950.2: 74,163-360,062 , GRCh38 chr17: 21,421,798-21,707,697 , GRCh37.p13 chr17: 21,325,110-21,517,390 LINC02693, RPL21P120, 5 more genes
    nsv5298241copy number variation1nstd204human GRCh38.p13 chr17: 21,543,743-21,575,619 , GRCh37.p13 chr17: 21,447,006-21,478,883 , GRCh37.p13 chr17|NW_003315950.2: 196,108-227,984 LINC02693
    nsv4767368inversion1nstd199human GRCh37 chr17: 21,254,966-25,335,261 , GRCh38.p12 chr17: 21,351,654-27,008,235 , KCNJ12, 36 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4747451copy number variation1nstd199human GRCh37 chr17: 21,327,887-25,309,307 , GRCh38.p12 chr17: 21,424,575-26,982,281 , LOC100533640, 34 more genes
    nsv4733169copy number variation1nstd199human GRCh37 chr17: 21,353,727-25,335,265 , GRCh38.p12 chr17: 21,450,415-27,008,239 , LOC100422478, 34 more genes
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