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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115959mobile element insertion1nstd186human GRCh37 chr15: 101,178,173-101,178,224 , GRCh38.p12 chr15: 100,637,968-100,638,019 ASB7
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv5977096insertion1nstd209human GRCh38 chr15: 100,600,551-100,600,551 , GRCh37.p13 chr15: 101,140,756-101,140,756 LINS1, ASB7
    nsv5976933insertion1nstd209human GRCh38 chr15: 100,611,484-100,611,484 , GRCh37.p13 chr15: 101,151,689-101,151,689 ASB7
    nsv5973246inversion1nstd209human GRCh38 chr15: 97,535,582-101,746,493 , GRCh37.p13 chr15: 98,078,812-102,286,696 , ALDH1A3, 71 more genes
    nsv5969771insertion1nstd209human GRCh38 chr15: 100,637,952-100,637,952 , GRCh37.p13 chr15: 101,178,157-101,178,157 ASB7
    nsv5928290copy number variation1nstd209human GRCh38 chr15: 100,620,512-100,620,603 , GRCh37.p13 chr15: 101,160,717-101,160,808 ASB7
    nsv5885435copy number variation1nstd209human GRCh38 chr15: 100,626,822-100,628,121 , GRCh37.p13 chr15: 101,167,027-101,168,326 ASB7
    nsv5874949copy number variation1nstd209human GRCh38 chr15: 100,608,338-100,610,037 , GRCh37.p13 chr15: 101,148,543-101,150,242 ASB7
    nsv5873479copy number variation1nstd209human GRCh38 chr15: 100,651,674-100,652,873 , GRCh37.p13 chr15: 101,191,879-101,193,078 ASB7
    nsv5872497copy number variation1nstd209human GRCh38 chr15: 100,558,297-100,609,738 , GRCh37.p13 chr15: 101,098,502-101,149,943 LINS1, ASB7, 3 more genes
    nsv5704437mobile element insertion1nstd211human GRCh38 chr15: 100,629,035-100,629,035 , GRCh37.p13 chr15: 101,169,240-101,169,240 ASB7
    nsv5703486mobile element insertion1nstd211human GRCh38 chr15: 100,614,761-100,614,761 , GRCh37.p13 chr15: 101,154,966-101,154,966 ASB7
    nsv5697741mobile element insertion2nstd211human GRCh38 chr15: 100,637,968-100,637,968 , GRCh37.p13 chr15: 101,178,173-101,178,173 ASB7
    nsv5672734copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 99,192,811-101,791,668 , GRCh38.p12 chr15: 98,649,582-101,251,463 ALDH1A3, IGF1R, 43 more genes
    nsv5585209copy number variation1nstd207human GRCh38 chr15: 100,620,512-100,620,603 , GRCh37.p13 chr15: 101,160,717-101,160,808 ASB7
    nsv5530885copy number variation1nstd206human GRCh38 chr15: 100,620,553-100,620,604 , GRCh37.p13 chr15: 101,160,758-101,160,809 ASB7
    nsv5530755copy number variation1nstd206human GRCh38 chr15: 100,198,183-100,600,807 , GRCh37.p13 chr15: 100,738,388-101,141,012 LOC102723335, LINS1, 9 more genes
    nsv5426546mobile element insertion1nstd206human GRCh38 chr15: 100,629,035-100,629,061 , GRCh37.p13 chr15: 101,169,240-101,169,266 ASB7
    nsv5417084mobile element insertion1nstd206human GRCh38 chr15: 100,637,968-100,638,019 , GRCh37.p13 chr15: 101,178,173-101,178,224 ASB7
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