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Items: 1 to 20 of 280

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7044965inversion1nstd229human GRCh38 chr7: 41,724,962-41,728,550 , GRCh37.p13 chr7: 41,764,560-41,768,148 INHBA-AS1
    nsv6837431copy number variation1nstd229human GRCh38 chr7: 41,766,501-41,778,000 , GRCh37.p13 chr7: 41,806,099-41,817,598 INHBA-AS1
    nsv6836095copy number variation1nstd229human GRCh38 chr7: 41,779,460-41,781,172 , GRCh37.p13 chr7: 41,819,058-41,820,770 INHBA-AS1
    nsv6831903copy number variation1nstd229human GRCh38 chr7: 41,774,631-41,779,331 , GRCh37.p13 chr7: 41,814,229-41,818,929 INHBA-AS1
    nsv6826114copy number variation1nstd229human GRCh38 chr7: 41,741,838-41,746,710 , GRCh37.p13 chr7: 41,781,436-41,786,308 INHBA-AS1
    nsv6824151copy number variation1nstd229human GRCh38 chr7: 41,718,813-41,719,752 , GRCh37.p13 chr7: 41,758,411-41,759,350 INHBA-AS1
    nsv6822949copy number variation1nstd229human GRCh38 chr7: 41,748,039-41,790,820 , GRCh37.p13 chr7: 41,787,637-41,830,418 INHBA-AS1
    nsv6821688copy number variation1nstd229human GRCh38 chr7: 41,759,134-41,759,233 , GRCh37.p13 chr7: 41,798,732-41,798,831 INHBA-AS1
    nsv6818590copy number variation1nstd229human GRCh38 chr7: 41,779,401-41,781,500 , GRCh37.p13 chr7: 41,818,999-41,821,098 INHBA-AS1
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6619655copy number variation1nstd223human GRCh38 chr7: 41,760,222-41,760,463 , GRCh37.p13 chr7: 41,799,820-41,800,061 INHBA-AS1
    nsv6613019copy number variation1nstd223human GRCh38 chr7: 41,719,014-41,719,777 , GRCh37.p13 chr7: 41,758,612-41,759,375 INHBA-AS1
    nsv6607892copy number variation1nstd223human GRCh38 chr7: 41,715,054-41,715,408 , GRCh37.p13 chr7: 41,754,652-41,755,006 INHBA-AS1
    nsv6603128copy number variation1nstd223human GRCh38 chr7: 41,779,460-41,781,169 , GRCh37.p13 chr7: 41,819,058-41,820,767 INHBA-AS1
    nsv6602838copy number variation1nstd223human GRCh38 chr7: 41,750,222-42,104,434 , GRCh37.p13 chr7: 41,789,820-42,144,033 GLI3, INHBA-AS1
    nsv6574607inversion1nstd223human GRCh38 chr7: 35,958,610-45,735,691 , GRCh37.p13 chr7: 35,998,220-45,775,290 RPS17P13, LOC105375252, 182 more genes
    nsv6569859inversion1nstd223human GRCh38 chr7: 41,747,162-41,748,744 , GRCh37.p13 chr7: 41,786,760-41,788,342 INHBA-AS1
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313509copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,778,439-50,228,656 , GRCh38.p12 chr7: 40,738,840-50,189,060 LINC01447, ABCA13, 142 more genes
    nsv6312346copy number variation1nstd102humanPathogenic GRCh37 chr7: 39,726,267-42,262,852 , GRCh38.p12 chr7: 39,686,668-42,223,253 HMGN2P30, GLI3, 31 more genes
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