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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099297copy number variation1nstd231human GRCh38.p12 chr1: 58,444,770-67,143,664 , GRCh37 chr1: 58,910,442-67,609,347 AK4, CYP2J2, 125 more genes
    nsv7099210copy number variation1nstd231human GRCh38.p12 chr1: 66,256,800-84,953,993 , GRCh37 chr1: 66,722,483-85,419,676 ACADM, COX6A1P1, 211 more genes
    nsv7095627copy number variation1nstd102humanPathogenic GRCh37 chr1: 61,548,464-67,861,772 , GRCh38.p12 chr1: 61,082,792-67,396,089 ALG6, MIR3116-2, 94 more genes
    nsv7095538copy number variation1nstd102humanPathogenic GRCh37 chr1: 65,299,551-67,861,772 , GRCh38.p12 chr1: 64,833,868-67,396,089 MRPS21P1, MIER1, 36 more genes
    nsv7055498inversion1nstd229human GRCh38 chr1: 66,514,766-73,182,042 , GRCh37.p13 chr1: 66,980,449-73,647,725 LINC02796, LOC105378789, 80 more genes
    nsv7054976inversion1nstd229human GRCh38 chr1: 66,778,824-69,400,485 , GRCh37.p13 chr1: 67,244,507-69,866,168 ELOCP18, MIR1262, 40 more genes
    nsv6653469copy number variation1nstd229human GRCh38 chr1: 66,773,156-66,776,508 , GRCh37.p13 chr1: 67,238,839-67,242,191 DYNLT5
    nsv6653373copy number variation1nstd229human GRCh38 chr1: 66,759,644-66,769,276 , GRCh37.p13 chr1: 67,225,327-67,234,959 DYNLT5
    nsv6652716copy number variation1nstd229human GRCh38 chr1: 66,759,864-66,765,048 , GRCh37.p13 chr1: 67,225,547-67,230,731 DYNLT5
    nsv6636512copy number variation1nstd102humanUncertain significance GRCh37 chr1: 66,815,031-67,319,280 , GRCh38.p12 chr1: 66,349,348-66,853,597 DNAI4, LOC105378776, 5 more genes
    nsv6542115inversion1nstd223human GRCh38 chr1: 61,925,268-71,371,290 , GRCh37.p13 chr1: 62,390,940-71,836,973 PATJ, GNG12-AS1, 142 more genes
    nsv6328088copy number variation1nstd223human GRCh38 chr1: 66,759,864-66,765,045 , GRCh37.p13 chr1: 67,225,547-67,230,728 DYNLT5
    nsv6326064copy number variation1nstd223human GRCh38 chr1: 66,768,731-66,769,086 , GRCh37.p13 chr1: 67,234,414-67,234,769 DYNLT5
    nsv6318758copy number variation1nstd223human GRCh38 chr1: 66,755,226-66,772,638 , GRCh37.p13 chr1: 67,220,909-67,238,321 DYNLT5
    nsv6313537copy number variation1nstd102humanUncertain significance GRCh37 chr1: 65,125,111-69,186,543 , GRCh38.p12 chr1: 64,659,428-68,720,860 RPE65, DNAJB6P4, 64 more genes
    nsv6254443mobile element insertion1nstd215human GRCh38 chr1: 66,769,962-66,769,962 , GRCh37.p13 chr1: 67,235,645-67,235,645 DYNLT5
    nsv6133717copy number variation1nstd213human GRCh37 chr1: 67,129,903-67,226,903 , GRCh38.p12 chr1: 66,664,220-66,761,220 SGIP1, DYNLT5
    nsv6133538copy number variation1nstd213human GRCh37 chr1: 67,129,905-67,226,901 , GRCh38.p12 chr1: 66,664,222-66,761,218 SGIP1, DYNLT5
    nsv5675636mobile element insertion2nstd211human GRCh38 chr1: 66,762,060-66,762,060 , GRCh37.p13 chr1: 67,227,743-67,227,743 DYNLT5
    nsv5394319mobile element insertion1nstd206human GRCh38 chr1: 66,762,060-66,762,111 , GRCh37.p13 chr1: 67,227,743-67,227,794 DYNLT5
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