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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5530193copy number variation1nstd206human GRCh38 chr16: 31,360,062-31,360,180 , GRCh37.p13 chr16: 31,371,383-31,371,501 LOC100422479, ITGAX
    nsv5525943copy number variation1nstd206human GRCh38 chr16: 31,379,644-31,379,750 , GRCh37.p13 chr16: 31,390,965-31,391,071 ITGAX
    nsv5519487copy number variation1nstd206human GRCh38 chr16: 31,326,014-31,405,175 , GRCh37.p13 chr16: 31,337,335-31,416,496 LOC100422479, ITGAD, 2 more genes
    nsv5040420inversion1nstd200human GRCh38 chr16: 29,736,418-31,610,189 , GRCh37.p13 chr16: 29,747,739-31,621,510 , ZNF668, 119 more genes
    nsv4994626copy number variation1nstd200human GRCh38 chr16: 31,326,014-31,405,175 , GRCh37.p13 chr16: 31,337,335-31,416,496 LOC100422479, ITGAX, 2 more genes
    nsv4879933inversion1nstd200human GRCh37 chr16: 29,747,739-31,621,510 , GRCh38.p12 chr16: 29,736,418-31,610,189 , LOC613038, 119 more genes
    nsv4864103copy number variation1nstd200human GRCh37 chr16: 31,390,965-31,391,071 , GRCh38.p12 chr16: 31,379,644-31,379,750 ITGAX
    nsv4864102copy number variation1nstd200human GRCh37 chr16: 31,337,335-31,416,496 , GRCh38.p12 chr16: 31,326,014-31,405,175 ITGAM, LOC100422479, 2 more genes
    nsv4751748insertion1nstd199human GRCh37 chr16: 31,373,782-31,373,782 , GRCh38.p12 chr16: 31,362,461-31,362,461 ITGAX
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729988copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,350,747-31,905,898 , GRCh38.p12 chr16: 30,339,426-31,894,577 VN1R3, HSD3B7, 89 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4670813copy number variation1nstd186human GRCh37 chr16: 31,380,443-31,380,684 , GRCh38.p12 chr16: 31,369,122-31,369,363 ITGAX
    nsv4620541copy number variation1nstd183human GRCh37 chr16: 31,380,443-31,380,684 , GRCh38.p12 chr16: 31,369,122-31,369,363 ITGAX
    nsv4530922copy number variation1nstd166human GRCh37.p13 chr16: 31,376,999-31,377,152 , GRCh38.p12 chr16: 31,365,678-31,365,831 ITGAX
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4416391copy number variation1nstd174human GRCh37 chr16: 31,338,462-31,424,425 , GRCh38.p12 chr16: 31,327,141-31,413,104 LOC100422479, ITGAM, 2 more genes
    nsv4322553inversion1nstd166human GRCh37.p13 chr16: 16,634,964-31,736,102 , GRCh38.p12 chr16: 16,541,107-31,724,781 , ALDOA, 403 more genes
    nsv4237908copy number variation1nstd166human GRCh37.p13 chr16: 31,384,996-31,385,066 , GRCh38.p12 chr16: 31,373,675-31,373,745 ITGAX
    nsv4236999copy number variation1nstd166human GRCh37.p13 chr16: 31,337,335-31,416,496 , GRCh38.p12 chr16: 31,326,014-31,405,175 ITGAM, ITGAD, 2 more genes
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