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Items: 1 to 20 of 303

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096096copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr21: 43,160,998-47,754,702 , GRCh38.p12 chr21: 41,740,838-46,334,788 TSPEAR, LINC01424, 158 more genes
    nsv7074266inversion1nstd229human GRCh38 chr21: 44,646,511-44,650,117 , GRCh37.p13 chr21|NW_004775435.1: 149,834-153,440 , GRCh37.p13 chr21: 46,066,428-46,070,034 KRTAP10-11, TSPEAR
    nsv7073104inversion1nstd229human GRCh38 chr21: 44,517,558-44,872,699 , GRCh37.p13 chr21|NW_004775435.1: 20,881-307,252 , GRCh37.p13 chr21: 45,937,441-46,223,846 KRTAP10-12, UBE2G2, 23 more genes
    nsv7064889inversion1nstd229human GRCh38 chr21: 41,632,756-44,900,321 , GRCh37.p13 chr21: 43,052,916-46,320,236 RNU6-1150P, LOC105372824, 123 more genes
    nsv7064241inversion1nstd229human GRCh38 chr21: 44,592,143-45,117,141 , GRCh37.p13 chr21: 46,223,847-46,537,056 KRTAP10-12, LINC01547, 27 more genes
    nsv7063843inversion1nstd229human GRCh38 chr21: 44,592,451-44,646,451 , GRCh37.p13 chr21|NW_004775435.1: 95,774-149,774 , GRCh37.p13 chr21: 46,012,332-46,066,368 KRTAP10-10, KRTAP10-6, 5 more genes
    nsv7031160copy number variation1nstd229human GRCh38 chr21: 44,571,074-44,737,926 , GRCh37.p13 chr21|NW_004775435.1: 74,397-241,247 , GRCh37.p13 chr21: 45,990,957-46,157,841 IMMTP1, KRTAP10-12, 15 more genes
    nsv7031037copy number variation1nstd229human GRCh38 chr21: 44,635,301-44,649,300 , GRCh37.p13 chr21|NW_004775435.1: 138,624-152,623 , GRCh37.p13 chr21: 46,055,218-46,069,217 KRTAP10-10, TSPEAR, 1 more genes
    nsv7030914copy number variation1nstd229human GRCh38 chr21: 44,640,663-44,644,914 , GRCh37.p13 chr21|NW_004775435.1: 143,986-148,237 , GRCh37.p13 chr21: 46,060,580-46,064,831 TSPEAR, KRTAP10-11
    nsv7023535copy number variation1nstd229human GRCh38 chr21: 44,620,531-44,663,614 , GRCh37.p13 chr21|NW_004775435.1: 123,854-166,937 , GRCh37.p13 chr21: 46,040,448-46,083,531 TSPEAR, KRTAP10-10, 4 more genes
    nsv7021657copy number variation1nstd229human GRCh38 chr21: 44,595,175-44,681,017 , GRCh37.p13 chr21|NW_004775435.1: 98,498-184,338 , GRCh37.p13 chr21: 46,015,066-46,100,618 KRTAP10-8, KRTAP12-4, 9 more genes
    nsv7018620copy number variation1nstd229human GRCh38 chr21: 44,473,788-44,670,842 , GRCh37.p13 chr21|NW_004775435.1: 1-174,165 , GRCh37.p13 chr21: 45,916,561-46,090,759 KRTAP10-2, KRTAP10-9, 18 more genes
    nsv6637798copy number variation1nstd102humanUncertain significance GRCh37 chr21: 45,843,864-46,176,026 , GRCh38.p12 chr21: 44,423,981-44,756,111 MTCYBP21, KRTAP10-13P, 28 more genes
    nsv6637666copy number variation1nstd102humanUncertain significance GRCh37 chr21: 45,727,195-46,161,988 , GRCh38.p12 chr21: 44,307,312-44,742,073 LRRC3-DT, MTND5P1, 30 more genes
    nsv6634428copy number variation1nstd102humanPathogenic GRCh37 chr21: 45,808,650-47,529,568 , GRCh38.p12 chr21: 44,388,767-46,109,654 KRTAP12-5P, MTCYBP21, 64 more genes
    nsv6626624copy number variation1nstd224human GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 , ATP5PO, 657 more genes
    nsv6599512inversion1nstd223human GRCh38 chr21: 43,690,612-45,780,509 , GRCh37.p13 chr21: 45,110,493-47,200,423 ADARB1, AIRE, 84 more genes
    nsv6599116inversion1nstd223human GRCh38 chr21: 43,689,244-45,912,414 , GRCh37.p13 chr21: 45,109,125-47,332,328 ADARB1, AIRE, 85 more genes
    nsv6543297copy number variation1nstd223human GRCh38 chr21: 44,647,599-44,648,064 , GRCh37.p13 chr21|NW_004775435.1: 150,922-151,387 , GRCh37.p13 chr21: 46,067,516-46,067,981 KRTAP10-11, TSPEAR
    nsv6538038copy number variation1nstd223human GRCh38 chr21: 44,571,001-44,737,900 , GRCh37.p13 chr21: 45,990,884-46,157,815 , GRCh37.p13 chr21|NW_004775435.1: 74,324-241,221 KRTAP10-12, KRTAP12-2, 15 more genes
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