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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049156inversion1nstd229human GRCh38 chr4: 70,056,642-70,056,739 , GRCh37.p13 chr4: 70,922,359-70,922,456 HTN1
    nsv7045939inversion1nstd229human GRCh38 chr4: 69,867,306-75,844,103 , GRCh37.p13 chr4: 70,733,024-76,765,256 , PF4V1, 99 more genes
    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
    nsv6750875copy number variation1nstd229human GRCh38 chr4: 70,044,501-70,144,100 , GRCh37.p13 chr4: 70,910,218-71,009,817 HTN1, CSN1S2BP, 1 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
    nsv6747159copy number variation1nstd229human GRCh38 chr4: 70,058,488-70,064,148 , GRCh37.p13 chr4: 70,924,205-70,929,865 HTN1
    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
    nsv6741823copy number variation1nstd229human GRCh38 chr4: 70,054,801-70,066,300 , GRCh37.p13 chr4: 70,920,518-70,932,017 CSN1S2AP, HTN1
    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
    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
    nsv6387664copy number variation1nstd223human GRCh38 chr4: 70,055,549-70,056,022 , GRCh37.p13 chr4: 70,921,266-70,921,739 HTN1
    nsv6385372copy number variation1nstd223human GRCh38 chr4: 70,054,301-70,055,200 , GRCh37.p13 chr4: 70,920,018-70,920,917 HTN1
    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
    nsv6379788copy number variation1nstd223human GRCh38 chr4: 70,051,201-70,052,500 , GRCh37.p13 chr4: 70,916,918-70,918,217 HTN1
    nsv6314916copy number variation1nstd102humanPathogenic GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218 MICOS10P4, SULT1B1, 274 more genes
    nsv6313740copy number variation1nstd102humanPathogenic GRCh37 chr4: 61,867,555-74,711,517 , GRCh38.p12 chr4: 61,001,837-73,845,800 CXCL8, UGT2A1, 175 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6135358copy number variation1nstd213human GRCh37 chr4: 70,890,000-71,450,001 , GRCh38.p12 chr4: 70,024,283-70,584,284 SMR3B, CSN1S2BP, 13 more genes
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