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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5449076copy number variation1nstd206human GRCh38 chr3: 52,454,193-52,454,319 , GRCh37.p13 chr3: 52,488,209-52,488,335 TNNC1, NISCH
    nsv5443022copy number variation1nstd206human GRCh38 chr3: 52,450,389-52,450,482 , GRCh37.p13 chr3: 52,484,405-52,484,498 TNNC1
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4911347copy number variation1nstd200human GRCh38 chr3: 51,769,352-52,724,007 , GRCh37.p13 chr3: 51,803,368-52,758,023 , ACY1, 55 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4790701copy number variation1nstd200human GRCh37 chr3: 51,803,368-52,758,023 , GRCh38.p12 chr3: 51,769,352-52,724,007 , SNORD19B, 55 more genes
    nsv4728314copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,975,459-52,561,678 , GRCh38.p12 chr3: 51,941,443-52,527,662 ABHD14A-ACY1, POC1A, 32 more genes
    nsv4679783copy number variation1nstd189human GRCh37.p13 chr3: 52,082,781-53,128,685 , GRCh38.p12 chr3: 52,048,765-53,094,669 , ALAS1, 50 more genes
    nsv4673975copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,247,306-53,069,942 , GRCh38.p12 chr3: 51,209,875-53,035,926 RRP9, LOC100301990, 76 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4453518copy number variation1nstd102humanPathogenic GRCh37 chr3: 52,195,134-52,869,037 , GRCh38.p12 chr3: 52,161,118-52,835,021 SNORD19B, TLR9, 42 more genes
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 UQCRC1, DHX30, 291 more genes
    nsv4090048copy number variation1nstd166human GRCh37.p13 chr3: 52,482,125-52,501,989 , GRCh38.p12 chr3: 52,448,109-52,467,973 , TNNC1, 1 more genes
    nsv4075953copy number variation1nstd166human GRCh37.p13 chr3: 52,488,209-52,488,335 , GRCh38.p12 chr3: 52,454,193-52,454,319 NISCH, TNNC1
    nsv3960017copy number variation1nstd168human GRCh38 chr3: 52,433,262-52,468,502 , GRCh37.p13 chr3: 52,467,278-52,502,518 , TNNC1, 2 more genes
    nsv3917135copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 51,406,905-55,073,516 , GRCh37 chr3: 51,431,865-55,098,476 , GRCh38 chr3: 51,394,434-55,064,449 ACY1, ALAS1, 96 more genes
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