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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5377484translocation1nstd200human GRCh38 chr3: 45,221,007-45,221,007 , GRCh38 chr3: 45,222,626-45,222,626 , GRCh37.p13 chr3: 45,262,499-45,262,499 , GRCh37.p13 chr3: 45,264,118-45,264,118 TMEM158
    nsv5377483translocation1nstd200human GRCh38 chr3: 45,223,026-45,223,026 , GRCh38 chr3: 45,220,999-45,220,999 , GRCh37.p13 chr3: 45,262,491-45,262,491 , GRCh37.p13 chr3: 45,264,518-45,264,518 TMEM158
    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
    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
    nsv4373432copy number variation1nstd173human GRCh37 chr3: 45,243,355-45,285,935 , GRCh38.p12 chr3: 45,201,863-45,244,443 TMEM158, LOC101928636
    nsv4368843copy number variation1nstd173human GRCh37 chr3: 45,241,165-45,285,935 , GRCh38.p12 chr3: 45,199,673-45,244,443 TMEM158, LOC101928636
    nsv4365275copy number variation2nstd173human GRCh37 chr3: 45,243,355-45,285,947 , GRCh38.p12 chr3: 45,201,863-45,244,455 TMEM158, LOC101928636
    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
    nsv4090166copy number variation1nstd166human GRCh37.p13 chr3: 45,267,729-45,267,791 , GRCh38.p12 chr3: 45,226,237-45,226,299 TMEM158
    nsv4075064copy number variation1nstd166human GRCh37.p13 chr3: 45,242,977-45,290,302 , GRCh38.p12 chr3: 45,201,485-45,248,810 TMEM158, LOC101928636
    nsv3921567copy number variation1nstd102humanUncertain significance NCBI36 chr3: 45,050,227-45,247,771 , GRCh37.p13 chr3: 45,075,223-45,272,767 , GRCh38.p12 chr3: 45,033,731-45,231,275 CDCP1, LOC101928636, 4 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
    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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