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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964204insertion1nstd209human GRCh38 chr1: 162,791,518-162,791,518 , GRCh37.p13 chr1: 162,761,308-162,761,308 HSD17B7
    nsv5689108mobile element insertion2nstd211human GRCh38 chr1: 162,791,532-162,791,532 , GRCh37.p13 chr1: 162,761,322-162,761,322 HSD17B7
    nsv5621074insertion1nstd207human GRCh38 chr1: 162,791,518-162,791,518 , GRCh37.p13 chr1: 162,761,308-162,761,308 HSD17B7
    nsv5415220copy number variation1nstd206human GRCh38 chr1: 162,791,823-162,791,908 , GRCh37.p13 chr1: 162,761,613-162,761,698 HSD17B7
    nsv5412634mobile element insertion1nstd206human GRCh38 chr1: 162,791,518-162,791,518 , GRCh37.p13 chr1: 162,761,308-162,761,308 HSD17B7
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5297103copy number variation1nstd204human GRCh38.p13 chr1: 162,801,581-162,817,848 , GRCh37.p13 chr1: 162,771,371-162,787,638 HSD17B7
    nsv5217420copy number variation1nstd204human GRCh38.p13 chr1: 162,804,062-162,817,453 , GRCh37.p13 chr1: 162,773,852-162,787,243 HSD17B7
    nsv5204319copy number variation1nstd204human GRCh38.p13 chr1: 162,787,883-162,789,006 , GRCh37.p13 chr1: 162,757,673-162,758,796 HSD17B7, DDR2
    nsv5077068mobile element insertion1nstd203human GRCh38 chr1: 162,791,517-162,791,532 , GRCh37.p13 chr1: 162,761,307-162,761,322 HSD17B7
    nsv5074561mobile element insertion1nstd203human GRCh38 chr1: 162,791,524-162,791,532 , GRCh37.p13 chr1: 162,761,314-162,761,322 HSD17B7
    nsv5069452mobile element insertion1nstd203human GRCh38 chr1: 162,791,518-162,791,532 , GRCh37.p13 chr1: 162,761,308-162,761,322 HSD17B7
    nsv5067980mobile element insertion1nstd203human GRCh38 chr1: 162,791,521-162,791,532 , GRCh37.p13 chr1: 162,761,311-162,761,322 HSD17B7
    nsv5064466mobile element insertion1nstd203human GRCh38 chr1: 162,791,520-162,791,532 , GRCh37.p13 chr1: 162,761,310-162,761,322 HSD17B7
    nsv5064401mobile element insertion1nstd203human GRCh38 chr1: 162,791,724-162,791,724 , GRCh37.p13 chr1: 162,761,514-162,761,514 HSD17B7
    nsv5064051mobile element insertion1nstd203human GRCh38 chr1: 162,791,522-162,791,532 , GRCh37.p13 chr1: 162,761,312-162,761,322 HSD17B7
    nsv5062463mobile element insertion1nstd203human GRCh38 chr1: 162,791,525-162,791,532 , GRCh37.p13 chr1: 162,761,315-162,761,322 HSD17B7
    nsv5062235mobile element insertion1nstd203human GRCh38 chr1: 162,791,523-162,791,532 , GRCh37.p13 chr1: 162,761,313-162,761,322 HSD17B7
    nsv5062146mobile element insertion1nstd203human GRCh38 chr1: 162,791,532-162,791,532 , GRCh37.p13 chr1: 162,761,322-162,761,322 HSD17B7
    nsv4781244copy number variation1nstd200human GRCh37 chr1: 162,771,373-162,787,637 , GRCh38.p12 chr1: 162,801,583-162,817,847 HSD17B7
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