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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554086sequence alteration1nstd206human GRCh38 chr17: 2,002,441-2,408,835 , GRCh37.p13 chr17: 1,905,735-2,312,129 SMG6, TSR1, 20 more genes
    nsv5307156copy number variation1nstd204human GRCh38.p13 chr17: 2,015,834-2,075,295 , GRCh37.p13 chr17: 1,919,128-1,978,589 SMG6, HIC1, 8 more genes
    nsv5287679copy number variation1nstd204human GRCh38.p13 chr17: 2,015,664-2,044,155 , GRCh37.p13 chr17: 1,918,958-1,947,449 LOC105371486, DPH1, 3 more genes
    nsv5280795copy number variation1nstd204human GRCh37.p13 chr17: 1,935,941-1,961,542 , GRCh38.p13 chr17: 2,032,647-2,058,248 DPH1, HIC1, 4 more genes
    nsv4864456copy number variation1nstd200human GRCh37 chr17: 1,919,149-1,978,568 , GRCh38.p12 chr17: 2,015,855-2,075,274 SMG6, OVCA2, 8 more genes
    nsv4768381copy number variation1nstd102humanPathogenic GRCh37 chr17: 84,287-2,468,384 , GRCh38.p12 chr17: 234,496-2,565,090 GLOD4, RTN4RL1, 67 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4679392copy number variation1nstd189human GRCh37.p13 chr17: 1,721,439-2,257,819 , GRCh38.p12 chr17: 1,818,145-2,354,525 DPH1, HIC1, 20 more genes
    nsv4675624copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-2,221,159 , GRCh38.p12 chr17: 150,732-2,317,865 HNRNPA1P16, RTN4RL1, 60 more genes
    nsv4675291copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,737,911-2,233,965 , GRCh38.p12 chr17: 1,834,617-2,330,671 SRR, MIR212, 18 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 SRR, DBIL5P, 196 more genes
    nsv4621159copy number variation1nstd183human GRCh37 chr17: 1,944,832-1,945,070 , GRCh38.p12 chr17: 2,041,538-2,041,776 OVCA2, DPH1
    nsv4457609copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,690,502-1,992,920 , GRCh38.p12 chr17: 1,787,208-2,089,626 OVCA2, SMG6, 11 more genes
    nsv4457568copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,501,331-2,832,123 , GRCh38.p12 chr17: 1,598,037-2,928,829 TSR1, LOC284009, 47 more genes
    nsv4368798copy number variation1nstd173human GRCh37 chr17: 1,485,295-2,355,965 , GRCh38.p12 chr17: 1,582,001-2,452,671 RPA1, MIR132, 35 more genes
    nsv4350781copy number variation1nstd102humanPathogenic GRCh37 chr17: 47,546-6,287,620 , GRCh38.p12 chr17: 197,755-6,384,300 SERPINF1, UBE2G1, 201 more genes
    nsv4250903copy number variation1nstd166human GRCh37.p13 chr17: 1,944,000-1,953,000 , GRCh38.p12 chr17: 2,040,706-2,049,706 DPH1, MIR132, 2 more genes
    nsv4240639copy number variation1nstd166human GRCh37.p13 chr17: 1,892,610-2,057,634 , GRCh38.p12 chr17: 1,989,316-2,154,340 MIR212, RTN4RL1, 9 more genes
    nsv4240251copy number variation1nstd166human GRCh37.p13 chr17: 1,934,705-1,949,060 , GRCh38.p12 chr17: 2,031,411-2,045,766 OVCA2, DPH1
    nsv4237808copy number variation1nstd166human GRCh37.p13 chr17: 1,485,414-2,431,916 , GRCh38.p12 chr17: 1,582,120-2,528,622 TLCD2, RN7SL624P, 35 more genes
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