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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096704copy number variation1nstd102humanUncertain significance GRCh37 chr3: 168,802,697-172,835,521 , GRCh38.p12 chr3: 169,084,909-173,117,731 GHSR, KLF7P1, 67 more genes
    nsv7057325inversion1nstd229human GRCh38 chr3: 170,134,629-173,143,661 , GRCh37.p13 chr3: 169,852,417-172,861,451 LINC02068, LOC107986052, 45 more genes
    nsv7047264inversion1nstd229human GRCh38 chr3: 168,346,425-172,414,638 , GRCh37.p13 chr3: 168,064,213-172,132,428 RNU4-38P, LINC01997, 60 more genes
    nsv6731942copy number variation1nstd229human GRCh38 chr3: 171,106,114-171,106,144 , GRCh37.p13 chr3: 170,823,903-170,823,933 MIR569, LOC105374216, 1 more genes
    nsv6730014copy number variation1nstd229human GRCh38 chr3: 171,104,973-171,105,031 , GRCh37.p13 chr3: 170,822,762-170,822,820 LOC105374216, MIR569, 1 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6628676copy number variation1nstd224human GRCh37 chr3: 170,715,711-170,861,559 , GRCh38.p12 chr3: 170,997,922-171,143,770 SLC2A2, TNIK, 2 more genes
    nsv6291110copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 168,118,411-179,867,071 , GRCh38.p12 chr3: 168,400,623-180,149,283 ACTL6A, ECT2, 141 more genes
    nsv6208667insertion2nstd214human GRCh37.p13 chr3: 170,822,762-170,822,762 , GRCh38 chr3: 171,104,973-171,104,973 TNIK, MIR569, 1 more genes
    nsv6134792copy number variation1nstd213human GRCh37 chr3: 169,810,000-174,480,001 , GRCh38.p12 chr3: 170,092,212-174,762,211 ECT2, SKIL, 56 more genes
    nsv5902612copy number variation1nstd209human GRCh38 chr3: 171,104,973-171,105,030 , GRCh37.p13 chr3: 170,822,762-170,822,819 TNIK, LOC105374216, 1 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5439222copy number variation1nstd206human GRCh38 chr3: 171,104,973-171,105,032 , GRCh37.p13 chr3: 170,822,762-170,822,821 TNIK, LOC105374216, 1 more genes
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4646644copy number variation1nstd186human GRCh37 chr3: 170,822,762-170,822,820 , GRCh38.p12 chr3: 171,104,973-171,105,031 TNIK, MIR569, 1 more genes
    nsv4550533insertion1nstd166human GRCh37.p13 chr3: 170,822,741-170,822,741 , GRCh38.p12 chr3: 171,104,952-171,104,952 TNIK, MIR569, 1 more genes
    nsv4550488insertion1nstd166human GRCh37.p13 chr3: 170,822,762-170,822,762 , GRCh38.p12 chr3: 171,104,973-171,104,973 TNIK, MIR569, 1 more genes
    nsv4521511copy number variation1nstd166human GRCh37.p13 chr3: 170,822,762-170,822,820 , GRCh38.p12 chr3: 171,104,973-171,105,031 TNIK, MIR569, 1 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
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