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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7041748inversion1nstd229human GRCh38 chr3: 72,070,390-75,778,215 , GRCh37.p13 chr3: 72,119,541-75,827,366 FTH1P23, LOC107986099, 66 more genes
    nsv6714371copy number variation1nstd229human GRCh38 chr3: 72,821,401-73,061,500 , GRCh37.p13 chr3: 72,870,552-73,110,651 GXYLT2, FTH1P23, 6 more genes
    nsv6712385copy number variation1nstd229human GRCh38 chr3: 66,065,527-73,237,527 , GRCh37.p13 chr3: 66,051,202-73,286,678 , RNA5SP136, 79 more genes
    nsv6704700copy number variation1nstd229human GRCh38 chr3: 73,030,566-73,084,965 , GRCh37.p13 chr3: 73,079,717-73,134,116 PPP4R2, EBLN2
    nsv6628813copy number variation1nstd224human GRCh37 chr3: 73,088,864-73,131,351 , GRCh38.p12 chr3: 73,039,713-73,082,200 EBLN2, PPP4R2
    nsv6371065copy number variation1nstd223human GRCh38 chr3: 73,032,060-73,146,367 , GRCh37.p13 chr3: 73,081,211-73,195,518 RNU6-557P, RNU2-64P, 3 more genes
    nsv6314751copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914 AKR1B1P2, COL8A1, 231 more genes
    nsv6134705copy number variation1nstd213human GRCh37 chr3: 66,270,000-87,730,001 , GRCh38.p12 chr3: 66,219,846-87,680,851 , AKR1B1P2, 187 more genes
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5033386inversion1nstd200human GRCh38 chr3: 66,830,019-82,426,887 , GRCh37.p13 chr3: 66,880,443-82,476,038 , HNRNPA3P6, 150 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924571copy number variation1nstd200human GRCh38 chr3: 73,032,060-73,146,371 , GRCh37.p13 chr3: 73,081,211-73,195,522 EBLN2, LOC107986098, 3 more genes
    nsv4924570copy number variation1nstd200human GRCh38 chr3: 73,030,566-73,084,965 , GRCh37.p13 chr3: 73,079,717-73,134,116 PPP4R2, EBLN2
    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
    nsv4728221copy number variation1nstd102humanUncertain significance GRCh37 chr3: 70,938,608-74,660,846 , GRCh38.p12 chr3: 70,889,457-74,611,695 CCDC137P1, LINC02047, 45 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
    nsv3922768copy number variation1nstd102humanPathogenic GRCh37 chr3: 64,746,924-78,459,248 , GRCh38 chr3: 64,761,248-78,410,098 , NCBI36 chr3: 64,721,964-78,541,938 RNU6-557P, LOC105377160, 147 more genes
    nsv3920193copy number variation1nstd102humanPathogenic GRCh37 chr3: 67,441,430-73,463,152 , NCBI36 chr3: 67,524,120-73,545,842 , GRCh38 chr3: 67,391,006-73,414,001 RNPC3P1, LOC105377162, 65 more genes
    nsv3917061copy number variation1nstd102humanPathogenic NCBI36 chr3: 68,940,430-75,092,800 , GRCh37.p13 chr3: 68,857,740-75,010,110 , GRCh38.p12 chr3: 68,808,589-74,960,959 RYBP, GXYLT2, 69 more genes
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