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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914877copy number variation1nstd209human GRCh38 chr10: 9,273,966-9,274,058 , GRCh37.p13 chr10: 9,315,929-9,316,021 LINC00709, LOC101928272
    nsv5698313mobile element insertion2nstd211human GRCh38 chr10: 9,284,563-9,284,563 , GRCh37.p13 chr10: 9,326,526-9,326,526 LINC00709, LOC101928272
    nsv5641136insertion1nstd207human GRCh38 chr10: 9,274,017-9,274,017 , GRCh37.p13 chr10: 9,315,980-9,315,980 LOC101928272, LINC00709
    nsv5593108copy number variation1nstd207human GRCh38 chr10: 9,273,966-9,274,058 , GRCh37.p13 chr10: 9,315,929-9,316,021 LINC00709, LOC101928272
    nsv5399900mobile element insertion1nstd206human GRCh38 chr10: 9,284,563-9,284,614 , GRCh37.p13 chr10: 9,326,526-9,326,577 LINC00709, LOC101928272
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv4969558copy number variation1nstd200human GRCh38 chr10: 9,255,873-9,275,947 , GRCh37.p13 chr10: 9,297,836-9,317,910 LOC101928272, LINC00709
    nsv4735651copy number variation1nstd199human GRCh37 chr10: 9,315,937-9,316,004 , GRCh38.p12 chr10: 9,273,974-9,274,041 LINC00709, LOC101928272
    nsv4680835copy number variation1nstd189human GRCh37.p13 chr10: 9,191,050-9,512,718 , GRCh38.p12 chr10: 9,149,087-9,470,755 , LINC00709, 2 more genes
    nsv4679952copy number variation1nstd189human GRCh37.p13 chr10: 9,239,135-9,513,591 , GRCh38.p12 chr10: 9,197,172-9,471,628 , LINC00709, 2 more genes
    nsv4679560copy number variation1nstd189human GRCh37.p13 chr10: 9,302,856-10,277,312 , GRCh38.p12 chr10: 9,260,893-10,235,349 , HSP90AB7P, 6 more genes
    nsv4679092copy number variation1nstd189human GRCh37.p13 chr10: 9,124,596-9,541,901 , GRCh38.p12 chr10: 9,082,633-9,499,938 , LINC00709, 2 more genes
    nsv4455884copy number variation1nstd102humanPathogenic GRCh37 chr10: 8,011,156-9,996,086 , GRCh38.p12 chr10: 7,969,193-9,954,123 LOC105376396, KRT8P37, 22 more genes
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 LOC105376357, LINC02649, 264 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4187958copy number variation1nstd166human GRCh37.p13 chr10: 9,325,399-9,325,464 , GRCh38.p12 chr10: 9,283,436-9,283,501 LINC00709, LOC101928272
    nsv4186310copy number variation1nstd166human GRCh37.p13 chr10: 9,297,836-9,317,910 , GRCh38.p12 chr10: 9,255,873-9,275,947 LOC101928272, LINC00709
    nsv4182083copy number variation1nstd166human GRCh37.p13 chr10: 9,318,366-9,318,578 , GRCh38.p12 chr10: 9,276,403-9,276,615 LOC101928272, LINC00709
    nsv3940103insertion1nstd167human GRCh37 chr10: 9,315,929-9,315,929 , GRCh38.p12 chr10: 9,273,966-9,273,966 LINC00709, LOC101928272
    nsv3924406copy number variation1nstd102humanPathogenic GRCh38 chr10: 69,261-19,184,047 , GRCh37 chr10: 224,406-19,472,976 , NCBI36 chr10: 105,201-19,512,982 WDR37, LOC105376364, 302 more genes
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