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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4450734copy number variation1nstd102humanPathogenic GRCh38 chr22: 30,612,853-30,615,807 , GRCh37 chr22: 31,008,840-31,011,794 TCN2
    nsv4684070copy number variation1nstd102humanPathogenic GRCh37 chr22: 31,018,955-31,019,070 , GRCh38.p12 chr22: 30,622,968-30,623,083 TCN2
    nsv6315194delins1nstd102humanPathogenic GRCh37 chr22: 31,012,077-31,014,228 , GRCh38 chr22: 30,616,090-30,618,241 TCN2
    nsv5564413copy number variation1nstd102humanUncertain significance GRCh37 chr22: 31,008,840-31,013,502 , GRCh38.p12 chr22: 30,612,853-30,617,515 TCN2
    nsv7023877copy number variation1nstd229human GRCh38 chr22: 30,618,633-30,621,767 , GRCh37.p13 chr22: 31,014,620-31,017,754 TCN2
    nsv5547833copy number variation1nstd206human GRCh38 chr22: 30,618,608-30,621,786 , GRCh37.p13 chr22: 31,014,595-31,017,773 TCN2
    nsv6209210copy number variation1nstd214human GRCh38 chr22: 30,623,703-30,623,876 , GRCh37.p13 chr22: 31,019,690-31,019,863 TCN2
    nsv6225195copy number variation1nstd214human GRCh38 chr22: 30,623,705-30,623,876 , GRCh37.p13 chr22: 31,019,692-31,019,863 TCN2
    nsv6212702copy number variation1nstd214human GRCh38 chr22: 30,623,707-30,623,876 , GRCh37.p13 chr22: 31,019,694-31,019,863 TCN2
    nsv6209619copy number variation1nstd214human GRCh38 chr22: 30,623,905-30,623,984 , GRCh37.p13 chr22: 31,019,892-31,019,971 TCN2
    nsv5595227copy number variation1nstd207human GRCh38 chr22: 30,623,787-30,623,862 , GRCh37.p13 chr22: 31,019,774-31,019,849 TCN2
    nsv5034408copy number variation1nstd200human GRCh38 chr22: 30,611,752-30,624,301 , GRCh37.p13 chr22: 31,007,739-31,020,288 TCN2
    nsv5956620copy number variation1nstd209human GRCh38 chr22: 30,623,952-30,624,063 , GRCh37.p13 chr22: 31,019,939-31,020,050 TCN2
    nsv4280201copy number variation1nstd166human GRCh37.p13 chr22: 31,014,997-31,017,677 , GRCh38.p12 chr22: 30,619,010-30,621,690 TCN2
    nsv3377879copy number variation1nstd162human GRCh38 chr22: 30,623,834-30,623,895 , GRCh37.p13 chr22: 31,019,821-31,019,882 TCN2
    esv3887326copy number variation1estd219human GRCh37 chr22: 31,014,414-31,017,848 , GRCh38.p12 chr22: 30,618,427-30,621,861 TCN2
    esv3647564copy number variation1estd214human GRCh37 chr22: 31,014,414-31,017,848 , GRCh38.p12 chr22: 30,618,427-30,621,861 TCN2
    nsv1136668copy number variation1nstd106human GRCh37 chr22: 31,019,697-31,019,862 , GRCh38.p12 chr22: 30,623,710-30,623,875 TCN2
    esv3235015copy number variation1estd209human GRCh37 chr22: 31,014,100-31,014,106 , GRCh38.p12 chr22: 30,618,113-30,618,119 TCN2
    esv3235012copy number variation1estd209human GRCh37 chr22: 31,011,504-31,011,506 , GRCh38.p12 chr22: 30,615,517-30,615,519 TCN2
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