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Items: 1 to 20 of 131

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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
    nsv7033295copy number variation1nstd229human GRCh38 chr20: 7,305,923-7,312,834 , GRCh37.p13 chr20: 7,286,570-7,293,481 LINC01751
    nsv7029690copy number variation1nstd229human GRCh38 chr20: 7,245,501-7,341,000 , GRCh37.p13 chr20: 7,226,148-7,321,647 LINC01751, LINC01428
    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
    nsv7027106copy number variation1nstd229human GRCh38 chr20: 7,282,090-7,302,242 , GRCh37.p13 chr20: 7,262,737-7,282,889 LINC01751
    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
    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
    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
    nsv6315526copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,178,539-11,848,383 , GRCh38.p12 chr20: 3,197,893-11,867,735 LRRN4, MCM8-AS1, 129 more genes
    nsv6315484copy number variation1nstd102humanUncertain significance GRCh37 chr20: 7,106,057-8,085,390 , GRCh38.p12 chr20: 7,125,410-8,104,743 LINC01428, LINC01751, 9 more genes
    nsv6291558copy number variation1nstd102humanUncertain significance GRCh37 chr20: 7,036,007-8,138,271 , GRCh38.p12 chr20: 7,055,360-8,157,624 HAO1, LOC105372518, 10 more genes
    nsv6134183copy number variation1nstd213human GRCh37 chr20: 6,650,000-9,380,001 , GRCh38.p12 chr20: 6,669,353-9,399,354 BMP2, PHKBP1, 18 more genes
    nsv6133808copy number variation1nstd213human GRCh37 chr20: 3,300,000-12,130,001 , GRCh38.p12 chr20: 3,319,353-12,149,353 BMP2, CDC25B, 126 more genes
    nsv5025114copy number variation1nstd200human GRCh38 chr20: 7,140,850-7,347,982 , GRCh37.p13 chr20: 7,121,497-7,328,629 LINC01428, LINC01751, 1 more genes
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