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Items: 1 to 20 of 233

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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
    nsv6724537copy number variation1nstd229human GRCh38 chr3: 170,366,650-170,373,768 , GRCh37.p13 chr3: 170,084,438-170,091,556 SKIL
    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
    nsv6560323inversion1nstd223human GRCh38 chr3: 170,366,009-170,366,439 , GRCh37.p13 chr3: 170,083,797-170,084,227 SKIL
    nsv6368917copy number variation1nstd223human GRCh38 chr3: 170,368,358-170,370,096 , GRCh37.p13 chr3: 170,086,146-170,087,884 SKIL
    nsv6359546copy number variation1nstd223human GRCh38 chr3: 170,386,194-170,389,377 , GRCh37.p13 chr3: 170,103,982-170,107,165 SKIL
    nsv6311968copy number variation1nstd102humanUncertain significance GRCh37 chr3: 169,482,388-170,130,102 , GRCh38.p12 chr3: 169,764,600-170,412,314 TRV-AAC1-1, SEC62, 19 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
    nsv6156238copy number variation1nstd214human GRCh38 chr3: 170,387,669-170,387,813 , GRCh37.p13 chr3: 170,105,457-170,105,601 SKIL
    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
    nsv5992363copy number variation1nstd212human GRCh38 chr3: 170,385,322-170,386,022 , GRCh37.p13 chr3: 170,103,110-170,103,810 SKIL
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5436981copy number variation1nstd206human GRCh38 chr3: 170,378,416-170,378,550 , GRCh37.p13 chr3: 170,096,204-170,096,338 SKIL
    nsv5099053mobile element insertion1nstd203human GRCh38 chr3: 170,387,726-170,387,759 , GRCh37.p13 chr3: 170,105,514-170,105,547 SKIL
    nsv5092123mobile element insertion1nstd203human GRCh38 chr3: 170,367,450-170,367,456 , GRCh37.p13 chr3: 170,085,238-170,085,244 SKIL
    nsv5090732mobile element insertion1nstd203human GRCh38 chr3: 170,387,933-170,387,957 , GRCh37.p13 chr3: 170,105,721-170,105,745 SKIL
    nsv5087416mobile element insertion1nstd203human GRCh38 chr3: 170,387,883-170,387,933 , GRCh37.p13 chr3: 170,105,671-170,105,721 SKIL
    nsv5084740mobile element insertion1nstd203human GRCh38 chr3: 170,387,759-170,387,774 , GRCh37.p13 chr3: 170,105,547-170,105,562 SKIL
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