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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7051957inversion1nstd229human GRCh38 chr3: 100,950,457-102,238,704 , GRCh37.p13 chr3: 100,669,301-101,957,548 RPL24, ACTR3P3, 22 more genes
    nsv6710291copy number variation1nstd229human GRCh38 chr3: 101,655,781-101,655,971 , GRCh37.p13 chr3: 101,374,625-101,374,815 ZBTB11
    nsv6553815inversion1nstd223human GRCh38 chr3: 101,662,971-101,663,615 , GRCh37.p13 chr3: 101,381,815-101,382,459 ZBTB11
    nsv6553521inversion1nstd223human GRCh38 chr3: 101,668,392-101,668,643 , GRCh37.p13 chr3: 101,387,236-101,387,487 ZBTB11
    nsv6543056inversion1nstd223human GRCh38 chr3: 101,673,856-101,674,069 , GRCh37.p13 chr3: 101,392,700-101,392,913 ZBTB11
    nsv6537526inversion1nstd223human GRCh38 chr3: 94,859,299-102,665,887 , GRCh37.p13 chr3: 94,578,143-102,384,731 OR5AC4P, LOC105373996, 112 more genes
    nsv6313516copy number variation1nstd102humanUncertain significance GRCh37 chr3: 101,191,611-101,938,521 , GRCh38.p12 chr3: 101,472,767-102,219,677 CEP97, ZBTB11-AS1, 15 more genes
    nsv6311846copy number variation1nstd102humanPathogenic GRCh37 chr3: 100,945,813-101,484,395 , GRCh38.p12 chr3: 101,226,969-101,765,551 IMPG2, ZBTB11-AS1, 15 more genes
    nsv6293214mobile element insertion1nstd186human GRCh37 chr3: 101,391,901-101,391,952 , GRCh38.p12 chr3: 101,673,057-101,673,108 ZBTB11
    nsv5685302mobile element insertion1nstd211human GRCh38 chr3: 101,673,057-101,673,057 , GRCh37.p13 chr3: 101,391,901-101,391,901 ZBTB11
    nsv5409992mobile element insertion1nstd206human GRCh38 chr3: 101,673,057-101,673,108 , GRCh37.p13 chr3: 101,391,901-101,391,952 ZBTB11
    nsv5236859copy number variation1nstd204human GRCh37.p13 chr3: 101,366,245-101,441,744 , GRCh38.p13 chr3: 101,647,401-101,722,900 RPL24, ZBTB11, 4 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034224inversion1nstd200human GRCh38 chr3: 94,859,289-102,665,887 , GRCh37.p13 chr3: 94,578,133-102,384,731 , LOC105374005, 114 more genes
    nsv4728581copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 95,563,096-102,371,126 , GRCh38.p12 chr3: 95,844,252-102,652,282 COL8A1, CPOX, 107 more genes
    nsv4552788insertion1nstd166human GRCh37.p13 chr3: 101,383,259-101,383,259 , GRCh38.p12 chr3: 101,664,415-101,664,415 ZBTB11
    nsv4546547insertion1nstd166human GRCh37.p13 chr3: 101,389,783-101,389,783 , GRCh38.p12 chr3: 101,670,939-101,670,939 ZBTB11
    nsv4520641copy number variation1nstd166human GRCh37.p13 chr3: 101,305,028-101,858,244 , GRCh38.p12 chr3: 101,586,184-102,139,400 , NXPE3, 11 more genes
    nsv4323076inversion1nstd166human GRCh37.p13 chr3: 100,669,301-101,957,545 , GRCh38.p12 chr3: 100,950,457-102,238,701 , CEP97, 23 more genes
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