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Items: 1 to 20 of 574

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6811443copy number variation1nstd229human GRCh38 chr6: 155,133,801-155,208,500 , GRCh37.p13 chr6: 155,454,935-155,529,634 TIAM2
    nsv6812083copy number variation1nstd229human GRCh38 chr6: 155,144,279-155,174,648 , GRCh37.p13 chr6: 155,465,413-155,495,782 TIAM2
    nsv6817782copy number variation1nstd229human GRCh38 chr6: 155,201,385-155,210,805 , GRCh37.p13 chr6: 155,522,519-155,531,939 TIAM2
    nsv6806954copy number variation1nstd229human GRCh38 chr6: 155,149,264-155,158,214 , GRCh37.p13 chr6: 155,470,398-155,479,348 TIAM2
    nsv6798177copy number variation1nstd229human GRCh38 chr6: 155,137,732-155,144,581 , GRCh37.p13 chr6: 155,458,866-155,465,715 TIAM2
    nsv6814529copy number variation1nstd229human GRCh38 chr6: 155,185,512-155,185,541 , GRCh37.p13 chr6: 155,506,646-155,506,675 TIAM2
    nsv6805754copy number variation1nstd229human GRCh38 chr6: 155,205,195-155,205,221 , GRCh37.p13 chr6: 155,526,329-155,526,355 TIAM2
    nsv6630681copy number variation1nstd224human GRCh37 chr6: 155,488,901-155,504,960 , GRCh38.p12 chr6: 155,167,767-155,183,826 TIAM2
    nsv6616240copy number variation1nstd223human GRCh38 chr6: 155,144,279-155,174,644 , GRCh37.p13 chr6: 155,465,413-155,495,778 TIAM2
    nsv6605004copy number variation1nstd223human GRCh38 chr6: 155,125,561-155,126,454 , GRCh37.p13 chr6: 155,446,695-155,447,588 TIAM2
    nsv6610251copy number variation1nstd223human GRCh38 chr6: 155,226,369-155,226,692 , GRCh37.p13 chr6: 155,547,503-155,547,826 TIAM2
    nsv5454855copy number variation1nstd206human GRCh38 chr6: 155,222,389-155,226,458 , GRCh37.p13 chr6: 155,543,523-155,547,592 TIAM2
    nsv5466105copy number variation1nstd206human GRCh38 chr6: 155,113,992-155,114,399 , GRCh37.p13 chr6: 155,435,126-155,435,533 TIAM2
    nsv6185541copy number variation1nstd214human GRCh38 chr6: 155,122,363-155,122,476 , GRCh37.p13 chr6: 155,443,497-155,443,610 TIAM2
    nsv6006722copy number variation1nstd212human GRCh38 chr6: 155,218,953-155,219,025 , GRCh37.p13 chr6: 155,540,087-155,540,159 TIAM2
    nsv4943546copy number variation1nstd200human GRCh38 chr6: 155,174,485-155,176,360 , GRCh37.p13 chr6: 155,495,619-155,497,494 TIAM2
    nsv4811031copy number variation1nstd200human GRCh37 chr6: 155,495,619-155,497,494 , GRCh38.p12 chr6: 155,174,485-155,176,360 TIAM2
    nsv4888501mobile element deletion1nstd200human GRCh38 chr6: 155,226,386-155,226,692 , GRCh37.p13 chr6: 155,547,520-155,547,826 TIAM2
    nsv4150732copy number variation1nstd166human GRCh37.p13 chr6: 155,470,398-155,479,343 , GRCh38.p12 chr6: 155,149,264-155,158,209 TIAM2
    nsv4524426copy number variation1nstd166human GRCh37.p13 chr6: 155,459,241-155,459,552 , GRCh38.p12 chr6: 155,138,107-155,138,418 TIAM2
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