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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046756inversion1nstd229human GRCh38 chr4: 69,813,493-69,820,306 , GRCh37.p13 chr4: 70,679,211-70,686,024 SULT1D1P
    nsv6755453copy number variation1nstd229human GRCh38 chr4: 68,793,720-69,854,262 , GRCh37.p13 chr4: 69,659,438-70,719,980 SPOPLP1, UGT2B4, 33 more genes
    nsv6754934copy number variation1nstd229human GRCh38 chr4: 69,791,659-69,794,489 , GRCh37.p13 chr4: 70,657,377-70,660,207 SULT1D1P
    nsv6754154copy number variation1nstd229human GRCh38 chr4: 69,695,734-70,544,125 , GRCh37.p13 chr4: 70,561,452-71,409,842 OPRPN, HTN3, 20 more genes
    nsv6751190copy number variation1nstd229human GRCh38 chr4: 69,813,676-69,841,348 , GRCh37.p13 chr4: 70,679,394-70,707,066 SULT1E1, SULT1D1P
    nsv6750872copy number variation1nstd229human GRCh38 chr4: 69,796,781-69,796,802 , GRCh37.p13 chr4: 70,662,499-70,662,520 SULT1D1P
    nsv6749752copy number variation1nstd229human GRCh38 chr4: 68,786,846-69,797,610 , GRCh37.p13 chr4: 69,652,564-70,663,328 UGT2A2, UGT2B10, 33 more genes
    nsv6748778copy number variation1nstd229human GRCh38 chr4: 69,775,074-70,688,486 , GRCh37.p13 chr4: 70,640,792-71,554,203 SULT1E1, SMR3A, 24 more genes
    nsv6747961copy number variation1nstd229human GRCh38 chr4: 69,813,866-69,830,567 , GRCh37.p13 chr4: 70,679,584-70,696,285 SULT1D1P
    nsv6746769copy number variation1nstd229human GRCh38 chr4: 69,087,431-73,565,096 , GRCh37.p13 chr4: 69,953,149-74,430,813 LOC642496, CSN2, 76 more genes
    nsv6741409copy number variation1nstd229human GRCh38 chr4: 69,753,787-70,216,995 , GRCh37.p13 chr4: 70,619,505-71,082,712 STATH, HTN1, 12 more genes
    nsv6636838copy number variation1nstd102humanUncertain significance GRCh37 chr4: 70,479,061-70,985,189 , GRCh38.p12 chr4: 69,613,343-70,119,472 HTN3, LOC105377269, 10 more genes
    nsv6636652copy number variation1nstd102humanUncertain significance GRCh37 chr4: 70,478,978-70,985,189 , GRCh38.p12 chr4: 69,613,260-70,119,472 CSN1S1, SULT1D1P, 10 more genes
    nsv6636557copy number variation1nstd102humanUncertain significance GRCh37 chr4: 69,661,413-70,724,847 , GRCh38.p12 chr4: 68,795,695-69,859,129 LOC100422029, LOC100422189, 33 more genes
    nsv6629776copy number variation1nstd224human GRCh37 chr4: 70,620,387-71,081,038 , GRCh38.p12 chr4: 69,754,669-70,215,321 , GRCh38.p12 chr4|NW_013171801.1: 1-236,512 CSN2, HTN1, 12 more genes
    nsv6629772copy number variation1nstd224human GRCh37 chr4: 70,264,026-70,672,152 , GRCh38.p12 chr4: 69,398,308-69,806,434 UGT2A1, UGT2B24P, 8 more genes
    nsv6394050copy number variation1nstd223human GRCh38 chr4: 69,791,301-69,792,200 , GRCh37.p13 chr4: 70,657,019-70,657,918 SULT1D1P
    nsv6390622copy number variation1nstd223human GRCh38 chr4: 69,813,052-69,813,645 , GRCh37.p13 chr4: 70,678,770-70,679,363 SULT1D1P
    nsv6383817copy number variation1nstd223human GRCh38 chr4: 68,950,068-69,844,927 , GRCh37.p13 chr4: 69,815,786-70,710,645 UGT2A1, SPOPLP1, 28 more genes
    nsv6383205copy number variation1nstd223human GRCh38 chr4: 69,043,346-70,093,612 , GRCh37.p13 chr4: 69,909,064-70,959,329 CSN2, LOC642496, 30 more genes
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