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Items: 1 to 20 of 1349

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140144insertion1nstd232human GRCh37.p13 chr3: 169,268,613-169,268,613 , GRCh38.p12 chr3: 169,550,825-169,550,825 MECOM
    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
    nsv7055024inversion1nstd229human GRCh38 chr3: 169,282,808-169,282,919 , GRCh37.p13 chr3: 169,000,596-169,000,707 LOC105374206, MECOM
    nsv7053016inversion1nstd229human GRCh38 chr3: 169,570,222-169,571,865 , GRCh37.p13 chr3: 169,288,010-169,289,653 MECOM
    nsv7052694inversion1nstd229human GRCh38 chr3: 169,543,807-169,548,093 , GRCh37.p13 chr3: 169,261,595-169,265,881 MECOM
    nsv7047264inversion1nstd229human GRCh38 chr3: 168,346,425-172,414,638 , GRCh37.p13 chr3: 168,064,213-172,132,428 RNU4-38P, LINC01997, 60 more genes
    nsv7042097inversion1nstd229human GRCh38 chr3: 169,337,634-169,534,639 , GRCh37.p13 chr3: 169,055,422-169,252,427 MECOM, RPL22P1, 1 more genes
    nsv6737377copy number variation1nstd229human GRCh38 chr3: 169,086,427-169,086,512 , GRCh37.p13 chr3: 168,804,215-168,804,300 MECOM
    nsv6734965copy number variation1nstd229human GRCh38 chr3: 169,613,622-169,617,694 , GRCh37.p13 chr3: 169,331,410-169,335,482 MECOM
    nsv6733570copy number variation1nstd229human GRCh38 chr3: 169,632,601-169,635,500 , GRCh37.p13 chr3: 169,350,389-169,353,288 MECOM
    nsv6732898copy number variation1nstd229human GRCh38 chr3: 169,438,642-169,453,520 , GRCh37.p13 chr3: 169,156,430-169,171,308 MECOM-AS1, MECOM
    nsv6732790copy number variation1nstd229human GRCh38 chr3: 169,525,171-169,530,574 , GRCh37.p13 chr3: 169,242,959-169,248,362 MECOM
    nsv6732755copy number variation1nstd229human GRCh38 chr3: 169,550,825-169,551,091 , GRCh37.p13 chr3: 169,268,613-169,268,879 MECOM
    nsv6732192copy number variation1nstd229human GRCh38 chr3: 169,283,066-169,289,693 , GRCh37.p13 chr3: 169,000,854-169,007,481 MECOM, LOC105374206
    nsv6731617copy number variation1nstd229human GRCh38 chr3: 169,240,134-169,250,330 , GRCh37.p13 chr3: 168,957,922-168,968,118 MECOM
    nsv6731384copy number variation1nstd229human GRCh38 chr3: 169,421,087-169,435,018 , GRCh37.p13 chr3: 169,138,875-169,152,806 MECOM
    nsv6731137copy number variation1nstd229human GRCh38 chr3: 169,642,171-169,645,513 , GRCh37.p13 chr3: 169,359,959-169,363,301 MECOM
    nsv6729989copy number variation1nstd229human GRCh38 chr3: 169,510,794-169,513,161 , GRCh37.p13 chr3: 169,228,582-169,230,949 MECOM
    nsv6729281copy number variation1nstd229human GRCh38 chr3: 169,472,489-169,477,381 , GRCh37.p13 chr3: 169,190,277-169,195,169 MECOM-AS1, MECOM
    nsv6729215copy number variation1nstd229human GRCh38 chr3: 169,543,278-169,550,219 , GRCh37.p13 chr3: 169,261,066-169,268,007 MECOM
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