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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7094223copy number variation1nstd102humanUncertain significance GRCh37 chr12: 862,732-2,800,365 , GRCh38.p12 chr12|NW_018654718.1: 1-1,039,315 , GRCh38.p12 chr12: 753,566-2,691,199 DCP1B, CACNA1C-AS2, 28 more genes
    nsv7094036copy number variation1nstd102humanUncertain significance GRCh37 chr12: 1,949,885-2,764,424 , GRCh38.p12 chr12|NW_018654718.1: 182,863-1,003,374 , GRCh38.p12 chr12: 1,840,719-2,655,258 CACNA1C-IT3, LAMP1P1, 8 more genes
    nsv7093964copy number variation1nstd102humanUncertain significance GRCh37 chr12: 2,016,586-2,558,301 , GRCh38.p12 chr12: 1,907,420-2,449,135 , GRCh38.p12 chr12|NW_018654718.1: 249,564-797,251 CACNA2D4, LINC00940, 7 more genes
    nsv7070399inversion1nstd229human GRCh38 chr12: 1,988,476-1,988,560 , GRCh37.p13 chr12: 2,097,642-2,097,726 CACNA1C, DCP1B
    nsv6914465copy number variation1nstd229human GRCh38 chr12: 1,235,301-2,087,900 , GRCh37.p13 chr12: 1,344,467-2,197,066 LINC00940, WNT5B, 18 more genes
    nsv6913361copy number variation1nstd229human GRCh38 chr12: 823,634-1,993,927 , GRCh37.p13 chr12: 932,800-2,103,093 WNT5B, LOC105369601, 19 more genes
    nsv6913101copy number variation1nstd229human GRCh38 chr12: 1,989,311-1,998,683 , GRCh37.p13 chr12: 2,098,477-2,107,849 DCP1B, CACNA1C
    nsv6912599copy number variation1nstd229human GRCh38 chr12: 1,966,301-1,968,700 , GRCh37.p13 chr12: 2,075,467-2,077,866 CACNA1C, DCP1B
    nsv6910273copy number variation1nstd229human GRCh38 chr12: 1,253,201-1,955,300 , GRCh37.p13 chr12: 1,362,367-2,064,466 LOC107987182, LOC105369601, 15 more genes
    nsv6908279copy number variation1nstd229human GRCh38 chr12: 1,754,201-1,955,300 , GRCh37.p13 chr12: 1,863,367-2,064,466 ADIPOR2, LOC105369602, 7 more genes
    nsv6907386copy number variation1nstd229human GRCh38 chr12: 1,961,851-1,968,453 , GRCh37.p13 chr12: 2,071,017-2,077,619 CACNA1C, DCP1B
    nsv6905242copy number variation1nstd229human GRCh38 chr12: 1,935,101-1,955,300 , GRCh37.p13 chr12: 2,044,267-2,064,466 DCP1B, LINC00940
    nsv6902420copy number variation1nstd229human GRCh38 chr12: 1,971,412-1,971,999 , GRCh37.p13 chr12: 2,080,578-2,081,165 CACNA1C, DCP1B
    nsv6902075copy number variation1nstd229human GRCh38 chr12: 1,829,770-2,201,668 , GRCh37.p13 chr12: 1,938,936-2,310,834 DCP1B, CACNA1C, 7 more genes
    nsv6898792copy number variation1nstd229human GRCh38 chr12: 1,976,208-1,987,989 , GRCh37.p13 chr12: 2,085,374-2,097,155 CACNA1C, DCP1B
    nsv6637549copy number variation1nstd102humanUncertain significance GRCh37 chr12: 2,056,363-2,801,698 , GRCh38.p12 chr12: 1,947,197-2,692,532 , GRCh38.p12 chr12|NW_018654718.1: 289,341-1,040,648 CACNA1C, DCP1B, 8 more genes
    nsv6637376copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,787-8,320,544 , GRCh38.p12 chr12: 64,621-8,167,948 GCSHP4, RNU7-1, 220 more genes
    nsv6637310copy number variation1nstd102humanPathogenic GRCh37 chr12: 817,514-2,205,439 , GRCh38.p12 chr12: 708,348-2,096,273 LOC101929432, FBXL14, 24 more genes
    nsv6637302copy number variation1nstd102humanUncertain significance GRCh37 chr12: 2,019,716-2,674,054 , GRCh38.p12 chr12|NW_018654718.1: 252,694-913,004 , GRCh38.p12 chr12: 1,910,550-2,564,888 CACNA1C-AS4, CACNA1C-IT1, 7 more genes
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