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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112772copy number variation1nstd102humanPathogenic GRCh37 chr17: 2,313,096-3,735,525 , GRCh38.p12 chr17: 2,409,802-3,832,231 LOC105371592, OR3A5P, 49 more genes
    nsv5140789mobile element insertion1nstd203human GRCh38 chr17: 3,419,822-3,419,852 , GRCh37.p13 chr17: 3,323,116-3,323,146 OR3A3
    nsv5023546copy number variation1nstd200human GRCh38 chr17: 2,625,215-3,955,356 , GRCh37.p13 chr17: 2,528,509-3,858,650 OR1D3P, OR1E1, 47 more genes
    nsv5015500copy number variation1nstd200human GRCh38 chr17: 3,417,696-3,424,798 , GRCh37.p13 chr17: 3,320,990-3,328,092 OR3A3
    nsv4851392copy number variation1nstd200human GRCh37 chr17: 3,320,989-3,328,092 , GRCh38.p12 chr17: 3,417,695-3,424,798 OR3A3
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675501copy number variation1nstd102humanLikely benign GRCh37 chr17: 3,146,183-3,646,235 , GRCh38.p12 chr17: 3,242,889-3,742,941 RPL21P125, OR1AC1P, 24 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
    nsv4624679copy number variation1nstd183human GRCh37 chr17: 3,269,095-3,357,216 , GRCh38.p12 chr17: 3,365,801-3,453,922 OR3A2, OR1E1, 5 more genes
    nsv4624532copy number variation1nstd183human GRCh37 chr17: 3,285,135-3,799,918 , GRCh38.p12 chr17: 3,381,841-3,896,624 CAMKK1, OR1E2, 22 more genes
    nsv4624320copy number variation1nstd183human GRCh37 chr17: 2,582,661-3,422,908 , GRCh38.p12 chr17: 2,679,367-3,519,614 MIR1253, OR3A4P, 30 more genes
    nsv4619263copy number variation1nstd183human GRCh37 chr17: 3,157,904-3,405,803 , GRCh38.p12 chr17: 3,254,610-3,502,509 OR3A1, OR3A3, 10 more genes
    nsv4457530copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,160,211-3,424,544 , GRCh38.p12 chr17: 3,256,917-3,521,250 OR3A5P, SPATA22, 11 more genes
    nsv4457369copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,288,124-3,441,645 , GRCh38.p12 chr17: 3,384,830-3,538,351 OR3A3, ASPA, 6 more genes
    nsv4380453copy number variation1nstd173human GRCh37 chr17: 2,944,084-3,526,637 , GRCh38.p12 chr17: 3,040,790-3,623,343 SPATA22, OR1P1, 23 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
    nsv4252379copy number variation1nstd166human GRCh37.p13 chr17: 3,298,000-3,333,000 , GRCh38.p12 chr17: 3,394,706-3,429,706 OR3A3, OR1E1
    nsv4244794copy number variation1nstd166human GRCh37.p13 chr17: 3,230,000-3,355,000 , GRCh38.p12 chr17: 3,326,706-3,451,706 OR3A1, OR3A2, 6 more genes
    nsv4236211copy number variation1nstd166human GRCh37.p13 chr17: 3,320,990-3,328,092 , GRCh38.p12 chr17: 3,417,696-3,424,798 OR3A3
    nsv3961610insertion1nstd168human GRCh38 chr17: 3,421,018-3,423,245 , GRCh37.p13 chr17: 3,324,312-3,326,539 OR3A3
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