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Items: 1 to 20 of 171

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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
    nsv5287664copy number variation1nstd204human GRCh37.p13 chr17: 2,161,395-2,257,994 , GRCh38.p13 chr17: 2,258,101-2,354,700 SGSM2, SMG6, 5 more genes
    nsv5157741mobile element insertion1nstd203human GRCh38 chr17: 2,305,234-2,305,251 , GRCh37.p13 chr17: 2,208,528-2,208,545 HNRNPA1P16, SRR
    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
    nsv4674958copy number variation1nstd102humanUncertain significance GRCh37 chr17: 2,111,786-2,344,649 , GRCh38.p12 chr17: 2,208,492-2,441,355 SRR, LOC284009, 10 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
    nsv4457845copy number variation1nstd102humanPathogenic GRCh37 chr17: 2,172,709-2,646,895 , GRCh38.p12 chr17: 2,269,415-2,743,601 RN7SL608P, MNT, 19 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
    nsv4457414copy number variation1nstd102humanUncertain significance GRCh37 chr17: 2,010,046-2,279,595 , GRCh38.p12 chr17: 2,106,752-2,376,301 SGSM2, LOC101927839, 9 more genes
    nsv4435942copy number variation1nstd102humanUncertain significance GRCh37 chr17: 2,173,896-2,414,920 , GRCh38.p12 chr17: 2,270,602-2,511,626 SNORD91A, LOC101927864, 9 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
    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
    nsv4233782copy number variation1nstd166human GRCh37.p13 chr17: 2,145,000-2,230,000 , GRCh38.p12 chr17: 2,241,706-2,326,706 SMG6, HNRNPA1P16, 2 more genes
    nsv3924746copy number variation1nstd102humanPathogenic NCBI36 chr17: 1,912,473-3,991,926 , GRCh38 chr17: 2,062,429-4,141,883 , GRCh37 chr17: 1,965,723-4,045,177 OR1D5, OR1E3, 70 more genes
    nsv3923943copy number variation1nstd102humanPathogenic NCBI36 chr17: 84,287-2,235,556 , GRCh37 chr17: 396,627-2,288,806 , GRCh38 chr17: 234,496-2,385,512 INPP5K, VPS53, 64 more genes
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