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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4167091copy number variation1nstd166human GRCh37.p13 chr7: 100,467,517-100,467,594 , GRCh38.p12 chr7: 100,869,895-100,869,972 TRIP6
    esv3382561copy number variation1estd59human NCBI36 chr7: 100,304,452-100,306,500 , GRCh37.p13 chr7: 100,466,516-100,468,564 , GRCh38.p12 chr7: 100,868,894-100,870,942 TRIP6
    nsv366952copy number variation1nstd6human NCBI35 chr7: 100,113,714-100,113,727 , GRCh37.p13 chr7: 100,469,063-100,469,076 , GRCh38.p12 chr7: 100,871,441-100,871,454 TRIP6
    nsv5637245insertion1nstd207human GRCh38 chr7: 100,869,605-100,869,605 , GRCh37.p13 chr7: 100,467,227-100,467,227 TRIP6
    esv2842666insertion1estd209human GRCh37 chr7: 100,467,975-100,467,975 , GRCh38.p12 chr7: 100,870,353-100,870,353 TRIP6
    esv2569082insertion1estd197human NCBI36 chr7: 100,305,911-100,305,911 , GRCh37.p13 chr7: 100,467,975-100,467,975 , GRCh38.p12 chr7: 100,870,353-100,870,353 TRIP6
    esv2248256insertion1estd194human NCBI36 chr7: 100,305,912-100,305,912 , GRCh37.p13 chr7: 100,467,976-100,467,976 , GRCh38.p12 chr7: 100,870,354-100,870,354 TRIP6
    esv1495284insertion1estd22human NCBI36 chr7: 100,307,571-100,307,571 , GRCh37.p13 chr7: 100,469,635-100,469,635 , GRCh38.p12 chr7: 100,872,013-100,872,013 TRIP6
    esv1460808insertion1estd22human NCBI36 chr7: 100,305,911-100,305,911 , GRCh37.p13 chr7: 100,467,975-100,467,975 , GRCh38.p12 chr7: 100,870,353-100,870,353 TRIP6
    esv1108252insertion1estd22human NCBI36 chr7: 100,307,762-100,307,762 , GRCh37.p13 chr7: 100,469,826-100,469,826 , GRCh38.p12 chr7: 100,872,204-100,872,204 TRIP6
    nsv355794insertion1nstd6human NCBI35 chr7: 100,112,627-100,112,627 , GRCh37.p13 chr7: 100,467,976-100,467,976 , GRCh38.p12 chr7: 100,870,354-100,870,354 TRIP6
    nsv2514320short tandem repeat3nstd128human GRCh37 chr7: 100,468,655-100,468,675 , GRCh38.p12 chr7: 100,871,033-100,871,053 TRIP6
    nsv2514532short tandem repeat6nstd128human GRCh37 chr7: 100,470,475-100,470,490 , GRCh38.p12 chr7: 100,872,853-100,872,868 TRIP6
    nsv2514531short tandem repeat1nstd128human GRCh37 chr7: 100,467,524-100,467,539 , GRCh38.p12 chr7: 100,869,902-100,869,917 TRIP6
    nsv4819776copy number variation1nstd200human GRCh37 chr7: 100,470,580-100,471,237 , GRCh38.p12 chr7: 100,872,958-100,873,615 TRIP6, SRRT
    nsv2514322short tandem repeat2nstd128human GRCh37 chr7: 100,471,148-100,471,166 , GRCh38.p12 chr7: 100,873,526-100,873,544 TRIP6, SRRT
    nsv3133217copy number variation1nstd151human GRCh37 chr7: 100,457,504-100,464,232 , GRCh38.p12 chr7: 100,859,882-100,866,610 TRIP6, MIR6875, 1 more genes
    nsv942871copy number variation1nstd84human GRCh37 chr7: 100,456,674-100,466,489 , GRCh38.p12 chr7: 100,859,052-100,868,867 TRIP6, SLC12A9, 1 more genes
    nsv944001copy number variation1nstd84human GRCh37 chr7: 100,464,762-100,469,344 , GRCh38.p12 chr7: 100,867,140-100,871,722 TRIP6, SLC12A9, 1 more genes
    nsv2514530short tandem repeat1nstd128human GRCh37 chr7: 100,464,287-100,464,306 , GRCh38.p12 chr7: 100,866,665-100,866,684 TRIP6, MIR6875, 1 more genes
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