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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144111copy number variation1nstd232human GRCh37.p13 chr19: 3,820,904-3,821,002 , GRCh38.p12 chr19: 3,820,906-3,821,004 ZFR2
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7060352inversion1nstd229human GRCh38 chr19: 3,851,263-4,364,229 , GRCh37.p13 chr19: 3,851,261-4,364,226 DAPK3, YJU2, 22 more genes
    nsv7058895inversion1nstd229human GRCh38 chr19: 3,826,710-3,826,842 , GRCh37.p13 chr19: 3,826,708-3,826,840 ZFR2
    nsv7017718copy number variation1nstd229human GRCh38 chr19: 3,856,998-3,866,112 , GRCh37.p13 chr19: 3,856,996-3,866,110 ZFR2
    nsv7016095copy number variation1nstd229human GRCh38 chr19: 3,800,801-3,805,000 , GRCh37.p13 chr19: 3,800,799-3,804,998 MATK, ZFR2
    nsv7015566copy number variation1nstd229human GRCh38 chr19: 3,841,185-3,850,866 , GRCh37.p13 chr19: 3,841,183-3,850,864 ZFR2
    nsv7014566copy number variation1nstd229human GRCh38 chr19: 3,865,885-3,872,141 , GRCh37.p13 chr19: 3,865,883-3,872,139 FTLP5, ZFR2
    nsv7013690copy number variation1nstd229human GRCh38 chr19: 3,826,176-3,829,527 , GRCh37.p13 chr19: 3,826,174-3,829,525 ZFR2
    nsv7013618copy number variation1nstd229human GRCh38 chr19: 3,854,101-3,859,700 , GRCh37.p13 chr19: 3,854,099-3,859,698 ZFR2
    nsv7012362copy number variation1nstd229human GRCh38 chr19: 3,857,336-3,859,612 , GRCh37.p13 chr19: 3,857,334-3,859,610 ZFR2
    nsv7008320copy number variation1nstd229human GRCh38 chr19: 3,847,191-3,854,904 , GRCh37.p13 chr19: 3,847,189-3,854,902 ZFR2
    nsv7007969copy number variation1nstd229human GRCh38 chr19: 3,820,675-3,823,978 , GRCh37.p13 chr19: 3,820,673-3,823,976 ZFR2
    nsv7007825copy number variation1nstd229human GRCh38 chr19: 3,854,108-3,859,752 , GRCh37.p13 chr19: 3,854,106-3,859,750 ZFR2
    nsv7007648copy number variation1nstd229human GRCh38 chr19: 3,848,112-3,857,188 , GRCh37.p13 chr19: 3,848,110-3,857,186 ZFR2
    nsv7007241copy number variation1nstd229human GRCh38 chr19: 3,800,901-3,805,100 , GRCh37.p13 chr19: 3,800,899-3,805,098 ZFR2, MATK
    nsv7007072copy number variation1nstd229human GRCh38 chr19: 3,805,642-3,813,755 , GRCh37.p13 chr19: 3,805,640-3,813,753 ZFR2
    nsv7001186copy number variation1nstd229human GRCh38 chr19: 3,854,683-3,859,327 , GRCh37.p13 chr19: 3,854,681-3,859,325 ZFR2
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