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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052163inversion1nstd229human GRCh38 chr3: 87,535,323-87,655,478 , GRCh37.p13 chr3: 87,584,473-87,704,628 APOOP2, PSMC1P6
    nsv6717445copy number variation1nstd229human GRCh38 chr3: 87,617,755-87,632,956 , GRCh37.p13 chr3: 87,666,905-87,682,106 PSMC1P6
    nsv6708327copy number variation1nstd229human GRCh38 chr3: 87,609,124-87,650,711 , GRCh37.p13 chr3: 87,658,274-87,699,861 PSMC1P6
    nsv6706542copy number variation1nstd229human GRCh38 chr3: 87,553,554-87,636,253 , GRCh37.p13 chr3: 87,602,704-87,685,403 PSMC1P6, APOOP2
    nsv6702725copy number variation1nstd229human GRCh38 chr3: 87,623,489-87,628,268 , GRCh37.p13 chr3: 87,672,639-87,677,418 PSMC1P6
    nsv6636809copy number variation1nstd102humanUncertain significance GRCh37 chr3: 86,841,601-87,862,816 , GRCh38.p12 chr3: 86,792,451-87,813,666 CHMP2B, POU1F1, 12 more genes
    nsv6549876inversion1nstd223human GRCh38 chr3: 87,629,101-87,629,548 , GRCh37.p13 chr3: 87,678,251-87,678,698 PSMC1P6
    nsv6375133copy number variation1nstd223human GRCh38 chr3: 87,631,673-87,632,630 , GRCh37.p13 chr3: 87,680,823-87,681,780 PSMC1P6
    nsv6314751copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914 AKR1B1P2, COL8A1, 231 more genes
    nsv6291335copy number variation1nstd102humanLikely benign GRCh37 chr3: 87,501,074-87,875,813 , GRCh38.p12 chr3: 87,451,924-87,826,663 HTR1F, RNU6-873P, 3 more genes
    nsv6135252copy number variation1nstd213human GRCh37 chr3: 87,020,000-88,110,001 , GRCh38.p12 chr3: 86,970,850-88,060,851 POU1F1, CHMP2B, 14 more genes
    nsv6134867copy number variation1nstd213human GRCh37 chr3: 87,430,000-88,000,001 , GRCh38.p12 chr3: 87,380,850-87,950,851 HTR1F, PSMC1P6, 4 more genes
    nsv6134705copy number variation1nstd213human GRCh37 chr3: 66,270,000-87,730,001 , GRCh38.p12 chr3: 66,219,846-87,680,851 , AKR1B1P2, 187 more genes
    nsv4929038copy number variation1nstd200human GRCh38 chr3: 86,784,014-87,815,346 , GRCh37.p13 chr3: 86,833,164-87,864,496 LOC105377196, VGLL3, 12 more genes
    nsv4927716copy number variation1nstd200human GRCh38 chr3: 87,631,673-87,632,630 , GRCh37.p13 chr3: 87,680,823-87,681,780 PSMC1P6
    nsv4924689copy number variation1nstd200human GRCh38 chr3: 87,628,544-87,628,732 , GRCh37.p13 chr3: 87,677,694-87,677,882 PSMC1P6
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4794154copy number variation1nstd200human GRCh37 chr3: 87,677,694-87,677,882 , GRCh38.p12 chr3: 87,628,544-87,628,732 PSMC1P6
    nsv4674591copy number variation1nstd102humanUncertain significance GRCh37 chr3: 86,841,600-87,862,816 , GRCh38.p12 chr3: 86,792,450-87,813,666 PSMC1P6, LOC105377196, 12 more genes
    nsv4568251inversion1nstd166human GRCh37.p13 chr3: 81,845,861-90,137,796 , GRCh38.p12 chr3: 81,796,710-90,088,646 POU1F1, CHMP2B, 54 more genes
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