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Items: 1 to 20 of 152

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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
    nsv7146580insertion1nstd232human GRCh37.p13 chr20: 5,098,310-5,098,310 , GRCh38.p12 chr20: 5,117,664-5,117,664 PCNA, PCNA-AS1
    nsv7145616copy number variation1nstd232human GRCh37.p13 chr20: 5,099,323-5,099,413 , GRCh38.p12 chr20: 5,118,677-5,118,767 PCNA, PCNA-AS1
    nsv7143269copy number variation1nstd232human GRCh37.p13 chr20: 5,096,008-5,096,093 , GRCh38.p12 chr20: 5,115,362-5,115,447 PCNA
    nsv7098816copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 3,005,123-5,547,871 , GRCh38.p12 chr20: 3,024,477-5,567,225 ADRA1D, AVP, 70 more genes
    nsv7095905copy number variation1nstd102humanUncertain significance GRCh37 chr20: 5,086,814-5,295,015 , GRCh38.p12 chr20: 5,106,168-5,314,369 UBE2D3P1, PCNA-AS1, 4 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
    nsv7095797copy number variation1nstd102humanUncertain significance GRCh37 chr20: 5,081,437-5,093,674 , GRCh38.p12 chr20: 5,100,791-5,113,028 PCNA, TMEM230
    nsv7074371inversion1nstd229human GRCh38 chr20: 2,515,505-5,510,656 , GRCh37.p13 chr20: 2,496,151-5,491,302 RPL19P1, DDRGK1, 87 more genes
    nsv7063954inversion1nstd229human GRCh38 chr20: 3,693,712-5,966,241 , GRCh37.p13 chr20: 3,674,359-5,946,887 GPCPD1, PANK2, 52 more genes
    nsv7060166inversion1nstd229human GRCh38 chr20: 2,999,965-6,521,256 , GRCh37.p13 chr20: 2,980,611-6,501,903 FASTKD5, LOC101929098, 86 more genes
    nsv7015435copy number variation1nstd229human GRCh38 chr20: 4,445,183-5,667,683 , GRCh37.p13 chr20: 4,425,830-5,648,329 LOC107985411, LOC105372510, 26 more genes
    nsv7014372copy number variation1nstd229human GRCh38 chr20: 5,080,312-5,185,028 , GRCh37.p13 chr20: 5,060,958-5,165,674 CDS2, PCNA-AS1, 3 more genes
    nsv7008977copy number variation1nstd229human GRCh38 chr20: 4,351,306-5,587,282 , GRCh37.p13 chr20: 4,331,953-5,567,928 LINC00658, GPCPD1, 26 more genes
    nsv7007847copy number variation1nstd229human GRCh38 chr20: 5,051,802-5,318,241 , GRCh37.p13 chr20: 5,032,448-5,298,887 UBE2D3P1, PROKR2, 5 more genes
    nsv7005000copy number variation1nstd229human GRCh38 chr20: 5,122,750-5,126,872 , GRCh37.p13 chr20: 5,103,396-5,107,518 PCNA, CDS2
    nsv6626572copy number variation1nstd224human GRCh37 chr20: 4,155,880-5,165,596 , GRCh38.p12 chr20: 4,175,233-5,184,950 SMOX, PRNT, 18 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
    nsv6134039copy number variation1nstd213human GRCh37 chr20: 4,990,000-5,290,001 , GRCh38.p12 chr20: 5,009,354-5,309,355 PCNA, CDS2, 7 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
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