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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7036489copy number variation1nstd229human GRCh38 chr20: 7,361,680-7,363,941 , GRCh37.p13 chr20: 7,342,327-7,344,588 LINC01706
    nsv7035410copy number variation1nstd229human GRCh38 chr20: 7,356,311-7,366,490 , GRCh37.p13 chr20: 7,336,958-7,347,137 LINC01706
    nsv7031098copy number variation1nstd229human GRCh38 chr20: 7,362,770-7,365,118 , GRCh37.p13 chr20: 7,343,417-7,345,765 LINC01706
    nsv7029085copy number variation1nstd229human GRCh38 chr20: 7,367,671-7,370,115 , GRCh37.p13 chr20: 7,348,318-7,350,762 LINC01706, MIR8062
    nsv7028502copy number variation1nstd229human GRCh38 chr20: 7,054,114-8,875,895 , GRCh37.p13 chr20: 7,034,761-8,856,542 RNU105B, RN7SL547P, 13 more genes
    nsv7027569copy number variation1nstd229human GRCh38 chr20: 6,878,271-7,512,436 , GRCh37.p13 chr20: 6,858,918-7,493,083 MIR8062, LINC01428, 2 more genes
    nsv7022729copy number variation1nstd229human GRCh38 chr20: 7,235,562-10,519,088 , GRCh37.p13 chr20: 7,216,209-10,499,736 MKKS, PHKBP1, 30 more genes
    nsv7022285copy number variation1nstd229human GRCh38 chr20: 7,364,473-7,377,712 , GRCh37.p13 chr20: 7,345,120-7,358,359 LINC01706, MIR8062
    nsv7022267copy number variation1nstd229human GRCh38 chr20: 7,358,468-7,365,776 , GRCh37.p13 chr20: 7,339,115-7,346,423 LINC01706
    nsv7021705copy number variation1nstd229human GRCh38 chr20: 6,985,576-7,806,363 , GRCh37.p13 chr20: 6,966,223-7,787,010 RN7SL547P, LINC01751, 4 more genes
    nsv7019880copy number variation1nstd229human GRCh38 chr20: 7,352,348-7,359,722 , GRCh37.p13 chr20: 7,332,995-7,340,369 LINC01706
    nsv7018264copy number variation1nstd229human GRCh38 chr20: 7,346,747-7,385,559 , GRCh37.p13 chr20: 7,327,394-7,366,206 MIR8062, LINC01706
    nsv7006847copy number variation1nstd229human GRCh38 chr20: 5,360,624-8,409,137 , GRCh37.p13 chr20: 5,341,270-8,389,784 TMX4, LINC00654, 38 more genes
    nsv7006828copy number variation1nstd229human GRCh38 chr20: 6,181,226-7,626,473 , GRCh37.p13 chr20: 6,161,873-7,607,120 LINC01428, LINC01751, 9 more genes
    nsv7005912copy number variation1nstd229human GRCh38 chr20: 6,516,774-7,854,747 , GRCh37.p13 chr20: 6,497,421-7,835,394 SRSF10P2, LOC105372518, 9 more genes
    nsv6637311copy number variation1nstd102humanUncertain significance GRCh37 chr20: 7,106,058-8,586,513 , GRCh38.p12 chr20: 7,125,411-8,605,866 LINC01706, PHKBP1, 11 more genes
    nsv6626788copy number variation1nstd224human GRCh37 chr20: 5,204,639-8,101,337 , GRCh38.p12 chr20: 5,223,993-8,120,690 BMP2, EIF4EP1, 39 more genes
    nsv6626610copy number variation1nstd224human GRCh37 chr20: 7,112,386-8,573,437 , GRCh38.p12 chr20: 7,131,739-8,592,790 TMX4, LINC01751, 11 more genes
    nsv6535032copy number variation1nstd223human GRCh38 chr20: 7,344,506-7,346,064 , GRCh37.p13 chr20: 7,325,153-7,326,711 LINC01706
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