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Items: 1 to 20 of 125

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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
    nsv7095879copy number variation2nstd102humanUncertain significance GRCh37 chr20: 1,959,939-6,760,201 , GRCh38.p12 chr20: 1,979,293-6,779,554 SLC23A2, TARDBPP1, 120 more genes
    nsv7072133inversion1nstd229human GRCh38 chr20: 6,757,358-6,773,948 , GRCh37.p13 chr20: 6,738,005-6,754,595 BMP2, LOC105372517
    nsv7007457copy number variation1nstd229human GRCh38 chr20: 6,602,913-6,805,086 , GRCh37.p13 chr20: 6,583,560-6,785,733 BMP2, LINC01713, 1 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
    nsv7003257copy number variation1nstd229human GRCh38 chr20: 6,773,389-6,822,115 , GRCh37.p13 chr20: 6,754,036-6,802,762 BMP2
    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
    nsv6530883copy number variation1nstd223human GRCh38 chr20: 6,767,001-6,768,300 , GRCh37.p13 chr20: 6,747,648-6,748,947 LOC105372517, BMP2
    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
    nsv6134314copy number variation1nstd213human GRCh37 chr20: 6,250,000-6,750,001 , GRCh38.p12 chr20: 6,269,353-6,769,354 BMP2, CASC20, 2 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
    nsv6134087copy number variation1nstd213human GRCh37 chr20: 6,430,000-7,080,001 , GRCh38.p12 chr20: 6,449,353-7,099,354 BMP2, CASC20, 2 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
    nsv4861822copy number variation1nstd200human GRCh37 chr20: 6,748,523-6,748,607 , GRCh38.p12 chr20: 6,767,876-6,767,960 LOC105372517, BMP2
    nsv4682046copy number variation1nstd102humanPathogenic GRCh37 chr20: 6,015,110-6,759,736 , GRCh38.p12 chr20: 6,034,464-6,779,089 CASC20, TARDBPP1, 8 more genes
    nsv4567566insertion1nstd166human GRCh37.p13 chr20: 6,751,232-6,751,232 , GRCh38.p12 chr20: 6,770,585-6,770,585 BMP2
    nsv4566492sequence alteration1nstd166human GRCh37.p13 chr20: 6,738,001-6,754,593 , GRCh38.p12 chr20: 6,757,354-6,773,946 BMP2, LOC105372517
    nsv4502117mobile element insertion1nstd166human GRCh37.p13 chr20: 6,758,139-6,758,139 , GRCh38.p12 chr20: 6,777,492-6,777,492 BMP2
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