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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7043343inversion1nstd229human GRCh38 chr3: 180,954,365-180,955,990 , GRCh37.p13 chr3: 180,672,153-180,673,778 FXR1
    nsv7040124inversion1nstd229human GRCh38 chr3: 180,556,738-181,601,284 , GRCh37.p13 chr3: 180,274,526-181,319,072 DNAJC19, FXR1, 16 more genes
    nsv6730758copy number variation1nstd229human GRCh38 chr3: 180,936,382-180,943,378 , GRCh37.p13 chr3: 180,654,170-180,661,166 FXR1
    nsv6727113copy number variation1nstd229human GRCh38 chr3: 180,901,501-180,911,400 , GRCh37.p13 chr3: 180,619,289-180,629,188 FXR1
    nsv6634512copy number variation1nstd102humanPathogenic GRCh38 chr3: 179,547,548-182,152,788 , GRCh37.p13 chr3: 179,265,336-181,870,576 LOC105374243, RNF13P1, 34 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6567572inversion1nstd223human GRCh38 chr3: 180,930,764-180,931,400 , GRCh37.p13 chr3: 180,648,552-180,649,188 FXR1
    nsv6556462inversion1nstd223human GRCh38 chr3: 180,920,747-180,921,295 , GRCh37.p13 chr3: 180,638,535-180,639,083 FXR1
    nsv6371942copy number variation1nstd223human GRCh38 chr3: 180,965,339-180,965,807 , GRCh37.p13 chr3: 180,683,127-180,683,595 FXR1
    nsv6371531copy number variation1nstd223human GRCh38 chr3: 180,912,101-180,913,200 , GRCh37.p13 chr3: 180,629,889-180,630,988 FXR1
    nsv6369753copy number variation1nstd223human GRCh38 chr3: 180,914,044-180,915,495 , GRCh37.p13 chr3: 180,631,832-180,633,283 FXR1
    nsv6365638copy number variation1nstd223human GRCh38 chr3: 180,980,567-180,984,250 , GRCh37.p13 chr3: 180,698,355-180,702,038 FXR1, DNAJC19
    nsv6362661copy number variation1nstd223human GRCh38 chr3: 180,951,684-180,960,882 , GRCh37.p13 chr3: 180,669,472-180,678,670 FXR1
    nsv6356574copy number variation1nstd223human GRCh38 chr3: 180,919,573-180,919,914 , GRCh37.p13 chr3: 180,637,361-180,637,702 FXR1
    nsv6311784copy number variation1nstd102humanPathogenic GRCh37 chr3: 180,332,709-180,707,390 , GRCh38.p12 chr3: 180,614,921-180,989,602 ACTBP16, RNF13P1, 9 more genes
    nsv6300393copy number variation1nstd186human GRCh37 chr3: 180,680,881-180,685,837 , GRCh38.p12 chr3: 180,963,093-180,968,049 FXR1
    nsv6298386copy number variation1nstd186human GRCh37 chr3: 180,699,512-180,699,600 , GRCh38.p12 chr3: 180,981,724-180,981,812 FXR1, DNAJC19
    nsv6297644copy number variation1nstd186human GRCh37 chr3: 180,678,146-180,679,148 , GRCh38.p12 chr3: 180,960,358-180,961,360 FXR1
    nsv6290246copy number variation1nstd102humanPathogenic GRCh37 chr3: 175,119,199-187,592,480 , GRCh38.p12 chr3: 175,401,410-187,874,692 RPL39L, MCF2L2, 220 more genes
    nsv6283714insertion1nstd214human GRCh38 chr3: 180,921,733-180,921,733 , GRCh37.p13 chr3: 180,639,521-180,639,521 FXR1
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