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Items: 1 to 20 of 191

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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
    nsv6915082copy number variation1nstd229human GRCh38 chr12: 2,021,482-2,074,965 , GRCh37.p13 chr12: 2,130,648-2,184,131 CACNA1C-IT2, CACNA1C-IT1, 1 more genes
    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
    nsv6905950copy number variation1nstd229human GRCh38 chr12: 2,047,145-2,049,724 , GRCh37.p13 chr12: 2,156,311-2,158,890 CACNA1C-IT2, CACNA1C
    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
    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
    nsv6621584copy number variation1nstd224human GRCh37 chr12: 2,085,982-2,316,127 , GRCh38.p12 chr12: 1,976,816-2,206,961 , GRCh38.p12 chr12|NW_018654718.1: 318,960-549,105 DCP1B, CACNA1C-IT2, 3 more genes
    nsv6621583copy number variation1nstd224human GRCh37 chr12: 2,022,196-2,668,570 , GRCh38.p12 chr12: 1,913,030-2,559,404 , GRCh38.p12 chr12|NW_018654718.1: 255,174-907,520 CACNA1C, CACNA2D4, 7 more genes
    nsv6621434copy number variation1nstd224human GRCh37 chr12: 1,848,264-2,570,803 , GRCh38.p12 chr12: 1,739,098-2,461,637 , GRCh38.p12 chr12|NW_018654718.1: 81,242-809,753 DCP1B, RPS4XP14, 13 more genes
    nsv6585425inversion1nstd223human GRCh38 chr12: 1,440,406-2,565,306 , GRCh37.p13 chr12: 1,549,572-2,674,472 LRTM2, LOC107984507, 20 more genes
    nsv6474911copy number variation1nstd223human GRCh38 chr12: 2,047,145-2,049,714 , GRCh37.p13 chr12: 2,156,311-2,158,880 CACNA1C-IT2, CACNA1C
    nsv6469563copy number variation1nstd223human GRCh38 chr12: 2,030,701-2,064,100 , GRCh37.p13 chr12: 2,139,867-2,173,266 CACNA1C, CACNA1C-IT2, 1 more genes
    nsv6309258copy number variation1nstd102humanUncertain significance GRCh37 chr12: 1,949,885-2,229,616 , GRCh38.p12 chr12|NW_018654718.1: 182,863-462,594 , GRCh38.p12 chr12: 1,840,719-2,120,450 CACNA1C-IT1, LINC00940, 5 more genes
    nsv6290254copy number variation1nstd102humanPathogenic GRCh37 chr12: 146,240-8,330,229 , GRCh38.p12 chr12: 45,740-8,177,633 CLEC4A, FBXL14, 220 more genes
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