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Items: 1 to 20 of 181

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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
    nsv7048483inversion1nstd229human GRCh38 chr3: 169,821,268-170,002,421 , GRCh37.p13 chr3: 169,539,056-169,720,209 SAMD7, FHL1P1, 5 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
    nsv6734554copy number variation1nstd229human GRCh38 chr3: 169,972,483-169,974,655 , GRCh37.p13 chr3: 169,690,271-169,692,443 SEC62
    nsv6721333copy number variation1nstd229human GRCh38 chr3: 169,972,484-169,974,651 , GRCh37.p13 chr3: 169,690,272-169,692,439 SEC62
    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
    nsv6565827inversion1nstd223human GRCh38 chr3: 169,986,777-169,987,415 , GRCh37.p13 chr3: 169,704,565-169,705,203 SEC62
    nsv6555884inversion1nstd223human GRCh38 chr3: 169,821,268-170,002,422 , GRCh37.p13 chr3: 169,539,056-169,720,210 SEC62, LRRC31, 5 more genes
    nsv6371117copy number variation1nstd223human GRCh38 chr3: 169,994,401-169,995,400 , GRCh37.p13 chr3: 169,712,189-169,713,188 SEC62
    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
    nsv6062518insertion1nstd212human GRCh38 chr3: 169,989,288-169,989,288 , GRCh37.p13 chr3: 169,707,076-169,707,076 SEC62
    nsv5679742mobile element insertion1nstd211human GRCh38 chr3: 169,977,231-169,977,231 , GRCh37.p13 chr3: 169,695,019-169,695,019 SEC62
    nsv5607378insertion1nstd207human GRCh38 chr3: 169,989,288-169,989,288 , GRCh37.p13 chr3: 169,707,076-169,707,076 SEC62
    nsv5544037insertion1nstd206human GRCh38 chr3: 169,977,231-169,977,231 , GRCh37.p13 chr3: 169,695,019-169,695,019 SEC62
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5449947copy number variation1nstd206human GRCh38 chr3: 169,980,818-169,981,207 , GRCh37.p13 chr3: 169,698,606-169,698,995 SEC62
    nsv5098974mobile element insertion1nstd203human GRCh38 chr3: 169,989,290-169,989,290 , GRCh37.p13 chr3: 169,707,078-169,707,078 SEC62
    nsv5096586mobile element insertion1nstd203human GRCh38 chr3: 169,989,274-169,989,288 , GRCh37.p13 chr3: 169,707,062-169,707,076 SEC62
    nsv5095317mobile element insertion1nstd203human GRCh38 chr3: 169,989,285-169,989,288 , GRCh37.p13 chr3: 169,707,073-169,707,076 SEC62
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