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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7145659copy number variation1nstd232human GRCh37.p13 chr4: 54,005,539-54,005,702 , GRCh38.p12 chr4: 53,139,372-53,139,535 SCFD2
    nsv7142666insertion1nstd232human GRCh37.p13 chr4: 53,980,004-53,980,004 , GRCh38.p12 chr4: 53,113,837-53,113,837 SCFD2
    nsv7056198inversion1nstd229human GRCh38 chr4: 53,142,625-53,142,649 , GRCh37.p13 chr4: 54,008,792-54,008,816 SCFD2
    nsv7050444inversion1nstd229human GRCh38 chr4: 53,283,097-53,298,920 , GRCh37.p13 chr4: 54,149,264-54,165,087 SCFD2
    nsv7049224inversion1nstd229human GRCh38 chr4: 52,910,236-52,914,467 , GRCh37.p13 chr4: 53,776,403-53,780,634 SCFD2
    nsv7044693inversion1nstd229human GRCh38 chr4: 53,283,207-53,293,215 , GRCh37.p13 chr4: 54,149,374-54,159,382 SCFD2
    nsv7042297inversion1nstd229human GRCh38 chr4: 53,139,217-53,268,069 , GRCh37.p13 chr4: 54,005,384-54,134,236 RNU6-310P, SCFD2
    nsv7041504inversion1nstd229human GRCh38 chr4: 53,181,120-53,241,847 , GRCh37.p13 chr4: 54,047,287-54,108,014 SCFD2
    nsv6737979copy number variation1nstd229human GRCh38 chr4: 52,928,691-52,930,842 , GRCh37.p13 chr4: 53,794,858-53,797,009 LOC101928658, SCFD2
    nsv6737628copy number variation1nstd229human GRCh38 chr4: 53,000,689-53,004,364 , GRCh37.p13 chr4: 53,866,856-53,870,531 SCFD2
    nsv6737596copy number variation1nstd229human GRCh38 chr4: 53,080,867-53,105,704 , GRCh37.p13 chr4: 53,947,034-53,971,871 SCFD2
    nsv6737279copy number variation1nstd229human GRCh38 chr4: 52,859,601-52,873,800 , GRCh37.p13 chr4: 53,725,768-53,739,967 SCFD2, RASL11B
    nsv6737217copy number variation1nstd229human GRCh38 chr4: 53,282,502-53,298,658 , GRCh37.p13 chr4: 54,148,669-54,164,825 SCFD2
    nsv6736636copy number variation1nstd229human GRCh38 chr4: 53,207,126-53,225,331 , GRCh37.p13 chr4: 54,073,293-54,091,498 SCFD2
    nsv6736558copy number variation1nstd229human GRCh38 chr4: 53,268,546-53,278,347 , GRCh37.p13 chr4: 54,134,713-54,144,514 SCFD2
    nsv6736521copy number variation1nstd229human GRCh38 chr4: 52,883,008-52,887,808 , GRCh37.p13 chr4: 53,749,175-53,753,975 SCFD2
    nsv6736149copy number variation1nstd229human GRCh38 chr4: 53,208,455-53,342,491 , GRCh37.p13 chr4: 54,074,622-54,208,658 RNU6-310P, SCFD2
    nsv6736093copy number variation1nstd229human GRCh38 chr4: 53,024,640-53,029,746 , GRCh37.p13 chr4: 53,890,807-53,895,913 SCFD2
    nsv6735265copy number variation1nstd229human GRCh38 chr4: 53,207,201-53,225,300 , GRCh37.p13 chr4: 54,073,368-54,091,467 SCFD2
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