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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094605copy number variation1nstd102humanUncertain significance GRCh37 chr16: 85,936,622-86,602,447 , GRCh38.p12 chr16: 85,903,016-86,568,841 LINC00917, RPL7AP63, 16 more genes
    nsv7064013inversion1nstd229human GRCh38 chr16: 86,255,920-86,256,028 , GRCh37.p13 chr16: 86,289,526-86,289,634 LINC01081
    nsv6997647copy number variation1nstd229human GRCh38 chr16: 86,234,961-86,263,779 , GRCh37.p13 chr16: 86,268,567-86,297,385 LINC01081
    nsv6995866copy number variation1nstd229human GRCh38 chr16: 86,239,385-86,244,532 , GRCh37.p13 chr16: 86,272,991-86,278,138 LINC01081
    nsv6993685copy number variation1nstd229human GRCh38 chr16: 86,250,715-86,251,010 , GRCh37.p13 chr16: 86,284,321-86,284,616 LINC01081
    nsv6993215copy number variation1nstd229human GRCh38 chr16: 86,249,803-86,276,644 , GRCh37.p13 chr16: 86,283,409-86,310,250 LINC01081
    nsv6992285copy number variation1nstd229human GRCh38 chr16: 86,204,359-86,226,735 , GRCh37.p13 chr16: 86,237,965-86,260,341 LINC01081
    nsv6990157copy number variation1nstd229human GRCh38 chr16: 86,226,505-86,282,016 , GRCh37.p13 chr16: 86,260,111-86,315,622 LINC01081
    nsv6988616copy number variation1nstd229human GRCh38 chr16: 86,244,082-86,246,174 , GRCh37.p13 chr16: 86,277,688-86,279,780 LINC01081
    nsv6987265copy number variation1nstd229human GRCh38 chr16: 86,245,374-86,268,330 , GRCh37.p13 chr16: 86,278,980-86,301,936 LINC01081
    nsv6986826copy number variation1nstd229human GRCh38 chr16: 86,248,388-86,275,494 , GRCh37.p13 chr16: 86,281,994-86,309,100 LINC01081
    nsv6983444copy number variation1nstd229human GRCh38 chr16: 86,234,301-86,266,700 , GRCh37.p13 chr16: 86,267,907-86,300,306 LINC01081
    nsv6983031copy number variation1nstd229human GRCh38 chr16: 86,224,939-86,230,383 , GRCh37.p13 chr16: 86,258,545-86,263,989 LINC01081
    nsv6982925copy number variation1nstd229human GRCh38 chr16: 86,247,320-86,247,623 , GRCh37.p13 chr16: 86,280,926-86,281,229 LINC01081
    nsv6978212copy number variation1nstd229human GRCh38 chr16: 86,234,601-86,266,300 , GRCh37.p13 chr16: 86,268,207-86,299,906 LINC01081
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6624025copy number variation1nstd224human GRCh37 chr16: 86,274,851-86,294,853 , GRCh38.p12 chr16: 86,241,245-86,261,247 LINC01081
    nsv6623942copy number variation1nstd224human GRCh37 chr16: 86,290,512-86,710,660 , GRCh38.p12 chr16: 86,256,906-86,677,054 LINC02135, FENDRR, 10 more genes
    nsv6623792copy number variation1nstd224human GRCh37 chr16: 86,274,142-86,295,059 , GRCh38.p12 chr16: 86,240,536-86,261,453 LINC01081
    nsv6623791copy number variation1nstd224human GRCh37 chr16: 86,239,081-86,258,892 , GRCh38.p12 chr16: 86,205,475-86,225,286 LINC01081
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