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Items: 1 to 20 of 155

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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
    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
    nsv5015522copy number variation1nstd200human GRCh38 chr17: 3,669,982-3,671,018 , GRCh37.p13 chr17: 3,573,276-3,574,312 P2RX5-TAX1BP3, EMC6
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4685740copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,394,299-3,632,836 , GRCh38.p12 chr17: 3,491,005-3,729,542 ASPA, SHPK, 14 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
    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
    nsv4457629copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,405,774-3,640,694 , GRCh38.p12 chr17: 3,502,480-3,737,400 LOC105371493, SHPK, 14 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
    nsv4247278copy number variation1nstd166human GRCh37.p13 chr17: 3,535,374-3,588,226 , GRCh38.p12 chr17: 3,632,080-3,684,932 CTNS, P2RX5, 7 more genes
    nsv4234127copy number variation1nstd166human GRCh37.p13 chr17: 3,569,884-3,570,615 , GRCh38.p12 chr17: 3,666,590-3,667,321 TAX1BP3, EMC6, 1 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
    nsv3923881copy number variation1nstd102humanPathogenic NCBI36 chr17: 48,539-4,989,051 , GRCh37.p13 chr17: 48,539-5,048,327 , GRCh38.p12 chr17: 198,748-5,145,032 CAMKK1, MIR6776, 177 more genes
    nsv3923152copy number variation1nstd102humanPathogenic NCBI36 chr17: 3,451,558-7,022,067 , GRCh38 chr17: 3,601,515-7,178,024 , GRCh37 chr17: 3,504,809-7,081,343 PSMB6, NUP88, 133 more genes
    nsv3922546copy number variation1nstd102humanPathogenic NCBI36 chr17: 525-5,779,421 , GRCh38 chr17: 150,732-5,935,377 , GRCh37 chr17: 525-5,838,697 CHRNE, SPNS2-AS1, 198 more genes
    nsv3921779copy number variation1nstd102humanPathogenic NCBI36 chr17: 87,039-4,585,577 , GRCh38 chr17: 237,248-4,735,533 , GRCh37 chr17: 396,627-4,638,828 ARRB2, RYKP1, 146 more genes
    nsv3921317copy number variation1nstd102humanLikely benign GRCh37 chr17: 3,071,664-3,756,276 , NCBI36 chr17: 3,018,414-3,703,025 , GRCh38 chr17: 3,168,370-3,852,982 HASPIN, ITGAE, 29 more genes
    nsv3920795copy number variation1nstd102humanPathogenic GRCh38 chr17: 2,062,380-5,258,340 , NCBI36 chr17: 1,912,424-5,102,359 , GRCh37 chr17: 1,965,674-5,161,635 LINC01996, OR3A1, 128 more genes
    nsv3919819copy number variation1nstd102humanPathogenic GRCh37 chr17: 50,690-4,168,935 , NCBI36 chr17: 48,539-4,115,684 , GRCh38 chr17: 198,748-4,265,640 LOC105371430, LOC642502, 125 more genes
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