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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961253insertion1nstd209human GRCh38 chr10: 27,518,899-27,518,899 , GRCh37.p13 chr10: 27,807,828-27,807,828 RAB18
    nsv5918423copy number variation1nstd209human GRCh38 chr10: 27,505,061-27,506,967 , GRCh37.p13 chr10: 27,793,990-27,795,896 RAB18
    nsv5914382copy number variation1nstd209human GRCh38 chr10: 27,312,316-36,846,398 , GRCh37.p13 chr10: 27,601,245-37,135,326 , RN7SL241P, 160 more genes
    nsv5861204copy number variation1nstd209human GRCh38 chr10: 27,505,008-27,507,007 , GRCh37.p13 chr10: 27,793,937-27,795,936 RAB18
    nsv5626001insertion1nstd207human GRCh38 chr10: 27,539,082-27,539,082 , GRCh37.p13 chr10: 27,828,011-27,828,011 RAB18
    nsv5539244insertion1nstd206human GRCh38 chr10: 27,518,898-27,518,898 , GRCh37.p13 chr10: 27,807,827-27,807,827 RAB18
    nsv5488988copy number variation1nstd206human GRCh38 chr10: 27,505,065-27,506,968 , GRCh37.p13 chr10: 27,793,994-27,795,897 RAB18
    nsv5483413copy number variation1nstd206human GRCh38 chr10: 27,507,920-27,513,222 , GRCh37.p13 chr10: 27,796,849-27,802,151 RAB18
    nsv5473925copy number variation1nstd206human GRCh38 chr10: 27,138,085-27,696,804 , GRCh37.p13 chr10: 27,427,014-27,985,733 TRIAP1P1, RNU2-24P, 15 more genes
    nsv5354229translocation1nstd200human GRCh38 chr10: 27,505,065-27,505,065 , GRCh38 chr10: 27,506,968-27,506,968 , GRCh37.p13 chr10: 27,793,994-27,793,994 , GRCh37.p13 chr10: 27,795,897-27,795,897 RAB18
    nsv5310437copy number variation1nstd204human GRCh38.p13 chr10: 27,505,062-27,506,968 , GRCh37.p13 chr10: 27,793,991-27,795,897 RAB18
    nsv5241089copy number variation1nstd204human GRCh38.p13 chr10: 27,505,408-27,507,007 , GRCh37.p13 chr10: 27,794,337-27,795,936 RAB18
    nsv4983900copy number variation1nstd200human GRCh38 chr10: 27,206,781-27,507,099 , GRCh37.p13 chr10: 27,495,710-27,796,028 RNU6-452P, ACBD5, 10 more genes
    nsv4975541copy number variation1nstd200human GRCh38 chr10: 27,542,395-27,543,869 , GRCh37.p13 chr10: 27,831,324-27,832,798 LINC02680, RAB18
    nsv4975540copy number variation1nstd200human GRCh38 chr10: 27,541,065-27,541,204 , GRCh37.p13 chr10: 27,829,994-27,830,133 LINC02680, RAB18
    nsv4975539copy number variation1nstd200human GRCh38 chr10: 27,514,975-27,515,091 , GRCh37.p13 chr10: 27,803,904-27,804,020 RAB18
    nsv4847881copy number variation1nstd200human GRCh37 chr10: 27,831,324-27,832,798 , GRCh38.p12 chr10: 27,542,395-27,543,869 LINC02680, RAB18
    nsv4846723copy number variation1nstd200human GRCh37 chr10: 27,829,994-27,830,133 , GRCh38.p12 chr10: 27,541,065-27,541,204 RAB18, LINC02680
    nsv4836507copy number variation1nstd200human GRCh37 chr10: 27,793,994-27,795,897 , GRCh38.p12 chr10: 27,505,065-27,506,968 RAB18
    nsv4729200copy number variation1nstd102humanUncertain significance GRCh37 chr10: 27,265,783-28,643,506 , GRCh38.p12 chr10: 26,976,854-28,354,577 RNU7-12P, SNORD130, 28 more genes
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