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Items: 1 to 20 of 356

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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
    nsv7073879inversion1nstd229human GRCh38 chr21: 44,573,831-44,599,189 , GRCh37.p13 chr21|NW_004775435.1: 77,154-102,512 , GRCh37.p13 chr21: 45,993,708-46,019,093 KRTAP10-5, KRTAP10-6, 3 more genes
    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
    nsv7069697inversion1nstd229human GRCh38 chr21: 44,591,757-44,637,941 , GRCh37.p13 chr21|NW_004775435.1: 95,080-141,264 , GRCh37.p13 chr21: 46,011,638-46,057,858 KRTAP10-6, KRTAP10-10, 4 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
    nsv7028757copy number variation1nstd229human GRCh38 chr21: 44,521,945-44,596,001 , GRCh37.p13 chr21|NW_004775435.1: 25,268-99,324 , GRCh37.p13 chr21: 45,941,828-46,015,892 KRTAP10-2, KRTAP10-6, 5 more genes
    nsv7020287copy number variation1nstd229human GRCh38 chr21: 44,573,888-44,637,477 , GRCh37.p13 chr21|NW_004775435.1: 77,211-140,800 , GRCh37.p13 chr21: 45,993,765-46,057,394 KRTAP10-9, TSPEAR, 6 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
    nsv6597860inversion1nstd223human GRCh38 chr21: 44,591,943-44,601,087 , GRCh37.p13 chr21|NW_004775435.1: 95,266-104,410 , GRCh37.p13 chr21: 46,011,824-46,021,002 TSPEAR, KRTAP10-6, 1 more genes
    nsv6596465inversion1nstd223human GRCh38 chr21: 44,591,225-44,600,923 , GRCh37.p13 chr21|NW_004775435.1: 94,548-104,246 , GRCh37.p13 chr21: 46,011,106-46,020,838 TSPEAR, KRTAP10-6, 1 more genes
    nsv6546352copy number variation1nstd223human GRCh38 chr21: 44,332,501-44,603,700 , GRCh37.p13 chr21: 45,752,384-45,916,560 TRPM2, MTND5P1, 17 more genes
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