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Items: 1 to 20 of 88

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051996inversion1nstd229human GRCh38 chr3: 43,186,996-45,060,828 , GRCh37.p13 chr3: 43,228,488-45,102,320 ABHD5, CLEC3B, 44 more genes
    nsv7038909inversion1nstd229human GRCh38 chr3: 40,520,096-45,093,302 , GRCh37.p13 chr3: 40,561,587-45,134,794 ABHD5, ZKSCAN7, 97 more genes
    nsv6715838copy number variation1nstd229human GRCh38 chr3: 44,865,575-44,869,293 , GRCh37.p13 chr3: 44,907,067-44,910,785 TMEM42
    nsv6706862copy number variation1nstd229human GRCh38 chr3: 43,255,168-44,930,739 , GRCh37.p13 chr3: 43,296,660-44,972,231 LOC101928529, ANO10, 40 more genes
    nsv6701441copy number variation1nstd229human GRCh38 chr3: 44,764,313-45,050,108 , GRCh37.p13 chr3: 44,805,805-45,091,600 TMEM42, ZDHHC3, 9 more genes
    nsv6366717copy number variation1nstd223human GRCh38 chr3: 44,759,283-44,881,010 , GRCh37.p13 chr3: 44,800,775-44,922,502 TMEM42, PPIAP18, 5 more genes
    nsv6134813copy number variation1nstd213human GRCh37 chr3: 44,650,000-45,860,001 , GRCh38.p12 chr3: 44,608,508-45,818,509 TGM4, CLEC3B, 35 more genes
    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
    nsv4924382copy number variation1nstd200human GRCh38 chr3: 44,759,215-44,881,079 , GRCh37.p13 chr3: 44,800,707-44,922,571 MIR564, KIF15, 5 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
    nsv4674744copy number variation1nstd102humanUncertain significance GRCh37 chr3: 44,444,902-45,413,927 , GRCh38.p12 chr3: 44,403,410-45,372,435 RPL12P44, TMEM42, 37 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
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3885169copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431 RNU6-243P, ZNF385D, 382 more genes
    nsv3883164copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787 ACAA1, ACVR2B, 344 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
    nsv3168877copy number variation1nstd158human GRCh37 chr3: 38,483,456-71,473,806 , GRCh38.p12 chr3: 38,441,965-71,424,655 , ACVR2B, 646 more genes
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