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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6310588copy number variation1nstd102humanPathogenic GRCh37 chr1: 150,776,487-150,779,291 , GRCh38.p12 chr1: 150,804,011-150,806,815 CTSK
    nsv6310589copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 150,778,175-150,778,629 , GRCh38.p12 chr1: 150,805,699-150,806,153 CTSK
    nsv4773986copy number variation1nstd200human GRCh37 chr1: 150,774,273-150,775,158 , GRCh38.p12 chr1: 150,801,797-150,802,682 CTSK
    esv1126935copy number variation1estd22human NCBI36 chr1: 149,046,179-149,046,187 , GRCh37.p13 chr1: 150,779,555-150,779,563 , GRCh38.p12 chr1: 150,807,079-150,807,087 CTSK
    nsv6641769copy number variation1nstd229human GRCh38 chr1: 150,805,205-150,805,634 , GRCh37.p13 chr1: 150,777,681-150,778,110 CTSK
    nsv4755068insertion1nstd199human GRCh37 chr1: 150,779,525-150,779,525 , GRCh38.p12 chr1: 150,807,049-150,807,049 CTSK
    nsv4537919insertion1nstd166human GRCh37.p13 chr1: 150,779,515-150,779,515 , GRCh38.p12 chr1: 150,807,039-150,807,039 CTSK
    nsv7057898inversion1nstd229human GRCh38 chr1: 150,804,269-150,806,291 , GRCh37.p13 chr1: 150,776,745-150,778,767 CTSK
    nsv1501371short tandem repeat15nstd128human GRCh37 chr1: 150,779,557-150,779,601 , GRCh38.p12 chr1: 150,807,081-150,807,125 CTSK
    nsv1501370short tandem repeat1nstd128human GRCh37 chr1: 150,768,348-150,768,378 , GRCh38.p12 chr1: 150,795,872-150,795,902 CTSK
    nsv1460805short tandem repeat11nstd128human GRCh37 chr1: 150,779,474-150,779,501 , GRCh38.p12 chr1: 150,806,998-150,807,025 CTSK
    nsv1501369short tandem repeat2nstd128human GRCh37 chr1: 150,766,871-150,766,892 , GRCh38.p12 chr1: 150,794,395-150,794,416 CTSK
    nsv1463674short tandem repeat2nstd128human GRCh37 chr1: 150,767,224-150,767,240 , GRCh38.p12 chr1: 150,794,748-150,794,764 CTSK
    nsv1462568short tandem repeat5nstd128human GRCh37 chr1: 150,777,686-150,777,701 , GRCh38.p12 chr1: 150,805,210-150,805,225 CTSK
    nsv1460803short tandem repeat3nstd128human GRCh37 chr1: 150,774,019-150,774,032 , GRCh38.p12 chr1: 150,801,543-150,801,556 CTSK
    nsv6310522copy number variation1nstd102humanUncertain significance GRCh37 chr1: 150,769,275-150,772,205 , GRCh38.p12 chr1: 150,796,799-150,799,729 CTSK, UBE2D3P3
    nsv6641768copy number variation1nstd229human GRCh38 chr1: 150,799,712-150,805,859 , GRCh37.p13 chr1: 150,772,188-150,778,335 CTSK, UBE2D3P3
    nsv6641767copy number variation1nstd229human GRCh38 chr1: 150,796,840-150,801,806 , GRCh37.p13 chr1: 150,769,316-150,774,282 CTSK, UBE2D3P3
    nsv6641683copy number variation1nstd229human GRCh38 chr1: 150,799,708-150,804,019 , GRCh37.p13 chr1: 150,772,184-150,776,495 CTSK, UBE2D3P3
    nsv4058053copy number variation1nstd166human GRCh37.p13 chr1: 150,780,983-150,781,114 , GRCh38.p12 chr1: 150,808,507-150,808,638 CTSK, ARNT
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