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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
    nsv6715907copy number variation1nstd229human GRCh38 chr3: 102,163,088-102,163,173 , GRCh37.p13 chr3: 101,881,932-101,882,017 LOC101929411
    nsv6712298copy number variation1nstd229human GRCh38 chr3: 102,094,861-102,357,029 , GRCh37.p13 chr3: 101,813,705-102,075,873 LOC107986105, LOC101929411
    nsv6537526inversion1nstd223human GRCh38 chr3: 94,859,299-102,665,887 , GRCh37.p13 chr3: 94,578,143-102,384,731 OR5AC4P, LOC105373996, 112 more genes
    nsv6361979copy number variation1nstd223human GRCh38 chr3: 102,164,029-102,164,440 , GRCh37.p13 chr3: 101,882,873-101,883,284 LOC101929411
    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
    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
    nsv4919222copy number variation1nstd200human GRCh38 chr3: 102,160,087-102,171,348 , GRCh37.p13 chr3: 101,878,931-101,890,192 LOC101929411
    nsv4797725copy number variation1nstd200human GRCh37 chr3: 101,878,931-101,890,192 , GRCh38.p12 chr3: 102,160,087-102,171,348 LOC101929411
    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
    nsv4674254copy number variation1nstd102humanPathogenic GRCh37 chr3: 101,812,245-112,174,485 , GRCh38.p12 chr3: 102,093,401-112,455,638 IFT57, LINC00636, 111 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
    nsv4087978copy number variation1nstd166human GRCh37.p13 chr3: 101,881,932-101,882,017 , GRCh38.p12 chr3: 102,163,088-102,163,173 LOC101929411
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3919242copy number variation1nstd102humanLikely benign GRCh38 chr3: 101,596,165-102,374,145 , NCBI36 chr3: 102,797,699-103,575,679 , GRCh37 chr3: 101,315,009-102,092,989 NFKBIZ, CEP97, 11 more genes
    nsv3918661copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683 MTCO2P29, GAP43, 401 more genes
    nsv3917160copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903 ATP6V1A, RPS10P4, 297 more genes
    nsv3911724copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 95,021,157-105,090,283 , GRCh37 chr3: 93,538,467-103,607,593 , GRCh38 chr3: 93,819,623-103,888,749 COL8A1, CPOX, 132 more genes
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