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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7068065inversion1nstd229human GRCh38 chr22: 27,585,838-32,538,391 , GRCh37.p13 chr22: 27,981,799-32,934,377 LOC105372995, NEFH, 147 more genes
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7035800copy number variation1nstd229human GRCh38 chr22: 30,480,363-30,697,469 , GRCh37.p13 chr22: 30,876,350-31,093,456 SIRPAP1, DUSP18, 10 more genes
    nsv7031681copy number variation1nstd229human GRCh38 chr22: 30,592,063-30,633,192 , GRCh37.p13 chr22: 30,988,050-31,029,179 PES1, TCN2, 1 more genes
    nsv7030435copy number variation1nstd229human GRCh38 chr22: 30,668,339-30,668,376 , GRCh37.p13 chr22: 31,064,326-31,064,363 SLC35E4, DUSP18
    nsv7029177copy number variation1nstd229human GRCh38 chr22: 30,651,020-30,653,284 , GRCh37.p13 chr22: 31,047,007-31,049,271 RPL13AP26, DUSP18, 1 more genes
    nsv7025034copy number variation1nstd229human GRCh38 chr22: 30,649,481-30,650,249 , GRCh37.p13 chr22: 31,045,468-31,046,236 SLC35E4, DUSP18
    nsv7024597copy number variation1nstd229human GRCh38 chr22: 30,662,322-30,665,673 , GRCh37.p13 chr22: 31,058,309-31,061,660 SLC35E4, DUSP18
    nsv7022516copy number variation1nstd229human GRCh38 chr22: 30,658,562-30,663,013 , GRCh37.p13 chr22: 31,054,549-31,059,000 SLC35E4, DUSP18
    nsv7021396copy number variation1nstd229human GRCh38 chr22: 30,649,501-30,650,200 , GRCh37.p13 chr22: 31,045,488-31,046,187 DUSP18, SLC35E4
    nsv7019326copy number variation1nstd229human GRCh38 chr22: 30,664,984-30,675,967 , GRCh37.p13 chr22: 31,060,971-31,071,954 DUSP18, SLC35E4
    nsv6638056copy number variation1nstd102humanUncertain significance GRCh37 chr22: 30,649,178-31,035,087 , GRCh38.p12 chr22: 30,253,189-30,639,100 GAL3ST1, SDC4P, 22 more genes
    nsv6551870copy number variation1nstd223human GRCh38 chr22: 30,649,481-30,650,246 , GRCh37.p13 chr22: 31,045,468-31,046,233 DUSP18, SLC35E4
    nsv6551060copy number variation1nstd223human GRCh38 chr22: 30,642,747-30,644,546 , GRCh37.p13 chr22: 31,038,734-31,040,533 SLC35E4
    nsv6549241copy number variation1nstd223human GRCh38 chr22: 30,659,456-30,688,376 , GRCh37.p13 chr22: 31,055,443-31,084,363 SLC35E4, DUSP18
    nsv6311263copy number variation1nstd102humanUncertain significance GRCh37 chr22: 29,083,885-34,046,674 , GRCh38.p12 chr22: 28,687,897-33,650,688 SNORD125, LOC107985533, 145 more genes
    nsv6275873copy number variation1nstd214human GRCh38 chr22: 30,644,705-30,644,757 , GRCh37.p13 chr22: 31,040,692-31,040,744 SLC35E4
    nsv6134210copy number variation1nstd213human GRCh37 chr22: 30,130,000-36,350,001 , GRCh38.p12 chr22: 29,734,011-35,953,953 HMOX1, LIF, 146 more genes
    nsv6134118copy number variation1nstd213human GRCh37 chr22: 27,870,000-35,640,001 , GRCh38.p12 chr22: 27,474,039-35,244,008 AP1B1, EWSR1, 172 more genes
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