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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5833357copy number variation1nstd209human GRCh38 chr2: 45,187-51,676 , GRCh37.p13 chr2: 45,187-51,676 FAM110C
    nsv5833260copy number variation1nstd209human GRCh38 chr2: 44,387-46,486 , GRCh37.p13 chr2: 44,387-46,486 FAM110C
    nsv5833205copy number variation1nstd209human GRCh38 chr2: 37,988-42,486 , GRCh37.p13 chr2: 37,988-42,486 FAM110C
    nsv5833204copy number variation1nstd209human GRCh38 chr2: 37,987-40,286 , GRCh37.p13 chr2: 37,987-40,286 FAM110C
    nsv5833012copy number variation1nstd209human GRCh38 chr2: 42,887-49,876 , GRCh37.p13 chr2: 42,887-49,876 FAM110C
    nsv5832679copy number variation1nstd209human GRCh38 chr2: 45,487-48,876 , GRCh37.p13 chr2: 45,487-48,876 FAM110C
    nsv5832625copy number variation1nstd209human GRCh38 chr2: 34,656-38,286 , GRCh37.p13 chr2: 34,656-38,286 FAM110C
    nsv5434332copy number variation1nstd206human GRCh38 chr2: 17,928-84,014 , GRCh37.p13 chr2: 17,928-84,014 FAM110C
    nsv5289044copy number variation1nstd204human GRCh38.p13 chr2: 32,185-51,766 , GRCh37.p13 chr2: 32,185-51,766 FAM110C
    nsv5213171copy number variation1nstd204human GRCh38.p13 chr2: 34,631-49,620 , GRCh37.p13 chr2: 34,631-49,620 FAM110C
    nsv5204248copy number variation1nstd204human GRCh38.p13 chr2: 32,201-37,400 , GRCh37.p13 chr2: 32,201-37,400 FAM110C
    nsv4904650copy number variation1nstd200human GRCh38 chr2: 12,872-48,349 , GRCh37.p13 chr2: 12,872-48,349 FAM110C
    nsv4891915copy number variation1nstd200human GRCh38 chr2: 41,994-43,666 , GRCh37.p13 chr2: 41,994-43,666 FAM110C
    nsv4891914copy number variation1nstd200human GRCh38 chr2: 41,321-45,151 , GRCh37.p13 chr2: 41,321-45,151 FAM110C
    nsv4788188copy number variation1nstd200human GRCh37 chr2: 36,575-191,015 , GRCh38.p12 chr2: 36,575-191,015 FAM110C, LOC105373324
    nsv4788187copy number variation1nstd200human GRCh37 chr2: 32,189-51,757 , GRCh38.p12 chr2: 32,189-51,757 FAM110C
    nsv4788186copy number variation1nstd200human GRCh37 chr2: 12,872-48,349 , GRCh38.p12 chr2: 12,872-48,349 FAM110C
    nsv4769849copy number variation1nstd200human GRCh37 chr2: 41,994-43,666 , GRCh38.p12 chr2: 41,994-43,666 FAM110C
    nsv4769848copy number variation1nstd200human GRCh37 chr2: 41,321-45,151 , GRCh38.p12 chr2: 41,321-45,151 FAM110C
    nsv4728591copy number variation1nstd102humanUncertain significance GRCh37 chr2: 12,770-1,126,253 , GRCh38.p12 chr2: 12,770-1,130,567 LOC105373351, LINC01875, 20 more genes
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