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Items: 1 to 20 of 339

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147695insertion1nstd232human GRCh37.p13 chr9: 132,621,534-132,621,534 , GRCh38.p12 chr9: 129,859,255-129,859,255 USP20
    nsv7098427copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,857,676-135,942,612 , GRCh38.p12 chr9: 129,095,397-133,067,225 ASS1, SETX, 86 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv6877080copy number variation1nstd229human GRCh38 chr9: 129,865,117-129,906,104 , GRCh37.p13 chr9: 132,627,396-132,668,383 FNBP1, USP20, 1 more genes
    nsv6869641copy number variation1nstd229human GRCh38 chr9: 129,831,525-129,941,719 , GRCh37.p13 chr9: 132,593,804-132,703,998 MIR6855, USP20, 2 more genes
    nsv6866387copy number variation1nstd229human GRCh38 chr9: 129,698,067-130,033,998 , GRCh37.p13 chr9: 132,460,346-132,796,277 USP20, FNBP1, 8 more genes
    nsv6862363copy number variation1nstd229human GRCh38 chr9: 129,841,059-129,846,183 , GRCh37.p13 chr9: 132,603,338-132,608,462 USP20
    nsv6861356copy number variation1nstd229human GRCh38 chr9: 129,677,229-130,203,315 , GRCh37.p13 chr9: 132,439,508-132,892,849 USP20, UBE2V1P4, 11 more genes
    nsv6637875copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,449,937-132,807,448 , GRCh38.p12 chr9: 129,687,658-130,045,169 PRRX2-AS1, USP20, 8 more genes
    nsv6633149copy number variation1nstd224human GRCh37 chr9: 132,541,344-132,978,477 , GRCh38.p12 chr9: 129,779,065-130,216,198 USP20, NCS1, 8 more genes
    nsv6454293copy number variation1nstd223human GRCh38 chr9: 129,855,203-130,025,275 , GRCh37.p13 chr9: 132,617,482-132,787,554 MIR6855, FNBP1, 1 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291261copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,523,763-132,604,808 , GRCh38.p12 chr9: 125,761,484-129,842,529 PTPA, AK1, 123 more genes
    nsv6279128insertion1nstd214human GRCh38 chr9: 129,875,859-129,875,859 , GRCh37.p13 chr9: 132,638,138-132,638,138 USP20
    nsv6278255insertion1nstd214human GRCh38 chr9: 129,859,255-129,859,255 , GRCh37.p13 chr9: 132,621,534-132,621,534 USP20
    nsv6240257mobile element insertion1nstd215human GRCh38 chr9: 129,857,665-129,857,665 , GRCh37.p13 chr9: 132,619,944-132,619,944 USP20
    nsv6142037copy number variation1nstd206human GRCh38 chr9: 129,875,859-129,875,924 , GRCh37.p13 chr9: 132,638,138-132,638,203 USP20
    nsv6137057copy number variation1nstd213human GRCh37 chr9: 130,360,000-135,460,001 , GRCh38.p12 chr9: 127,597,721-132,584,614 CRAT, GLE1, 145 more genes
    nsv6123887insertion1nstd186human GRCh37 chr9: 132,621,533-132,621,533 , GRCh38.p12 chr9: 129,859,254-129,859,254 USP20
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