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Items: 1 to 20 of 683

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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
    nsv7137772copy number variation1nstd232human GRCh37.p13 chr20: 3,238,625-3,238,759 , GRCh38.p12 chr20: 3,257,979-3,258,113 DNAAF9
    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
    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
    nsv7095551copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,063,276-3,903,941 , GRCh38.p12 chr20: 3,082,630-3,923,294 PANK2, MAVS, 31 more genes
    nsv7075829inversion1nstd229human GRCh38 chr20: 3,256,437-3,256,490 , GRCh37.p13 chr20: 3,237,083-3,237,136 DNAAF9
    nsv7074371inversion1nstd229human GRCh38 chr20: 2,515,505-5,510,656 , GRCh37.p13 chr20: 2,496,151-5,491,302 RPL19P1, DDRGK1, 87 more genes
    nsv7068018inversion1nstd229human GRCh38 chr20: 1,903,309-3,817,737 , GRCh37.p13 chr20: 1,883,955-3,798,384 PCED1A, UBOX5-AS1, 62 more genes
    nsv7066949inversion1nstd229human GRCh38 chr20: 3,264,635-3,264,729 , GRCh37.p13 chr20: 3,245,281-3,245,375 DNAAF9
    nsv7062374inversion1nstd229human GRCh38 chr20: 3,378,829-3,383,596 , GRCh37.p13 chr20: 3,359,476-3,364,243 DNAAF9
    nsv7060166inversion1nstd229human GRCh38 chr20: 2,999,965-6,521,256 , GRCh37.p13 chr20: 2,980,611-6,501,903 FASTKD5, LOC101929098, 86 more genes
    nsv7059255inversion1nstd229human GRCh38 chr20: 3,405,567-3,405,619 , GRCh37.p13 chr20: 3,386,214-3,386,266 DNAAF9
    nsv7017951copy number variation1nstd229human GRCh38 chr20: 3,293,070-3,438,954 , GRCh37.p13 chr20: 3,273,716-3,419,601 LOC101618237, RNU6-1019P, 4 more genes
    nsv7016010copy number variation1nstd229human GRCh38 chr20: 3,394,959-3,395,270 , GRCh37.p13 chr20: 3,375,606-3,375,917 DNAAF9
    nsv7015700copy number variation1nstd229human GRCh38 chr20: 3,277,265-3,299,483 , GRCh37.p13 chr20: 3,257,911-3,280,130 LOC101618237, DNAAF9
    nsv7014841copy number variation1nstd229human GRCh38 chr20: 3,396,390-3,402,311 , GRCh37.p13 chr20: 3,377,037-3,382,958 DNAAF9
    nsv7014277copy number variation1nstd229human GRCh38 chr20: 3,378,722-3,379,499 , GRCh37.p13 chr20: 3,359,369-3,360,146 DNAAF9
    nsv7012966copy number variation1nstd229human GRCh38 chr20: 3,281,257-3,281,315 , GRCh37.p13 chr20: 3,261,903-3,261,961 DNAAF9
    nsv7012363copy number variation1nstd229human GRCh38 chr20: 3,260,766-3,266,615 , GRCh37.p13 chr20: 3,241,412-3,247,261 DNAAF9
    nsv7010860copy number variation1nstd229human GRCh38 chr20: 3,191,107-3,407,328 , GRCh37.p13 chr20: 3,171,753-3,387,975 ITPA, DNAAF9, 5 more genes
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