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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901805copy number variation1nstd209human GRCh38 chr3: 167,911,293-167,911,865 , GRCh37.p13 chr3: 167,629,081-167,629,653 LRRC77P
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5441546copy number variation1nstd206human GRCh38 chr3: 167,911,293-167,911,909 , GRCh37.p13 chr3: 167,629,081-167,629,697 LRRC77P
    nsv5437521copy number variation1nstd206human GRCh38 chr3: 167,914,846-167,914,940 , GRCh37.p13 chr3: 167,632,634-167,632,728 LRRC77P
    nsv5387850copy number variation1nstd186human GRCh37 chr3: 167,629,069-167,629,710 , GRCh38.p12 chr3: 167,911,281-167,911,922 LRRC77P
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4924829copy number variation1nstd200human GRCh38 chr3: 167,911,239-167,911,976 , GRCh37.p13 chr3: 167,629,027-167,629,764 LRRC77P
    nsv4920582copy number variation1nstd200human GRCh38 chr3: 167,906,363-167,908,369 , GRCh37.p13 chr3: 167,624,151-167,626,157 LRRC77P
    nsv4804977copy number variation1nstd200human GRCh37 chr3: 167,614,414-167,614,516 , GRCh38.p12 chr3: 167,896,626-167,896,728 LRRC77P
    nsv4452794copy number variation1nstd102humanPathogenic GRCh37 chr3: 165,603,872-168,796,960 , GRCh38.p12 chr3: 165,886,084-169,079,172 MTND4P17, LINC02082, 31 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4111616copy number variation1nstd166human GRCh37.p13 chr3: 167,624,151-167,626,157 , GRCh38.p12 chr3: 167,906,363-167,908,369 LRRC77P
    nsv4110587copy number variation1nstd166human GRCh37.p13 chr3: 167,632,634-167,632,728 , GRCh38.p12 chr3: 167,914,846-167,914,940 LRRC77P
    nsv4108539copy number variation1nstd166human GRCh37.p13 chr3: 167,629,081-167,629,654 , GRCh38.p12 chr3: 167,911,293-167,911,866 LRRC77P
    nsv4107830copy number variation1nstd166human GRCh37.p13 chr3: 167,568,826-167,639,923 , GRCh38.p12 chr3: 167,851,038-167,922,135 MEMO1P3, LRRC77P
    nsv4103792copy number variation1nstd166human GRCh37.p13 chr3: 167,614,414-167,614,516 , GRCh38.p12 chr3: 167,896,626-167,896,728 LRRC77P
    nsv4092706copy number variation1nstd166human GRCh37.p13 chr3: 167,636,894-167,636,953 , GRCh38.p12 chr3: 167,919,106-167,919,165 LRRC77P
    nsv3919833copy number variation1nstd102humanPathogenic GRCh38 chr3: 158,141,556-172,788,324 , NCBI36 chr3: 159,342,039-173,988,808 , GRCh37 chr3: 157,859,345-172,506,114 NMD3, TRV-AAC1-1, 173 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918784copy number variation1nstd102humanPathogenic GRCh37 chr3: 147,160,353-178,240,319 , GRCh38 chr3: 147,442,566-178,522,531 , NCBI36 chr3: 148,643,043-179,723,013 LOC105374167, LOC105374187, 394 more genes
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