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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5885134copy number variation1nstd209human GRCh38 chr1: 143,707,729-148,368,205 , GRCh37.p13 chr1|NW_003871055.3: 523,142-5,183,618 , TRN-GTT22-1, 183 more genes
    nsv5881371copy number variation1nstd209human GRCh38 chr1: 145,648,753-147,971,330 , GRCh37.p13 chr1|NW_003871055.3: 2,464,166-4,786,743 , RNVU1-6, 72 more genes
    nsv5694082mobile element insertion2nstd211human GRCh38 chr1: 147,641,941-147,641,941 , GRCh37.p13 chr1: 147,113,740-147,113,740 , GRCh37.p13 chr1|NW_003871055.3: 4,457,354-4,457,354 ACP6
    nsv5665280inversion1nstd207human GRCh38 chr1: 146,323,908-149,356,055 , GRCh37.p13 chr1|NW_003871055.3: 3,139,321-6,171,468 , BCL9, 98 more genes
    nsv5618176insertion1nstd207human GRCh38 chr1: 147,652,919-147,652,919 , GRCh37.p13 chr1|NW_003871055.3: 4,468,332-4,468,332 , GRCh37.p13 chr1: 147,124,726-147,124,726 ACP6
    nsv5611541insertion1nstd207human GRCh38 chr1: 147,653,119-147,653,119 , GRCh37.p13 chr1|NW_003871055.3: 4,468,532-4,468,532 ACP6
    nsv5429813copy number variation1nstd206human GRCh38 chr1: 147,640,561-147,640,680 , GRCh37.p13 chr1|NW_003871055.3: 4,455,974-4,456,093 , GRCh37.p13 chr1: 147,112,360-147,112,479 ACP6
    nsv5407843mobile element insertion1nstd206human GRCh38 chr1: 147,641,941-147,641,992 , GRCh37.p13 chr1: 147,113,740-147,113,791 , GRCh37.p13 chr1|NW_003871055.3: 4,457,354-4,457,405 ACP6
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5293881copy number variation1nstd204human GRCh38.p13 chr1: 147,631,810-147,632,420 , GRCh37.p13 chr1|NW_003871055.3: 4,447,223-4,447,833 , GRCh37.p13 chr1: 147,103,608-147,104,216 ACP6
    nsv5212061copy number variation1nstd204human GRCh38.p13 chr1: 147,600,000-147,642,760 , GRCh37.p13 chr1: 147,071,792-147,114,560 , GRCh37.p13 chr1|NW_003871055.3: 4,415,413-4,458,173 ACP6, BCL9
    nsv5201820copy number variation1nstd204human GRCh38.p13 chr1: 146,991,801-148,070,900 , GRCh37.p13 chr1|NW_003871055.3: 3,807,214-4,886,313 , TRN-GTT9-2, 37 more genes
    nsv5201284copy number variation1nstd204human GRCh38.p13 chr1: 147,632,006-147,670,590 , GRCh37.p13 chr1: 147,103,804-147,142,712 , GRCh37.p13 chr1|NW_003871055.3: 4,447,419-4,486,003 ACP6
    nsv5200304copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,500,972-147,851,297 , GRCh38.p12 chr1: 145,430,980-148,371,305 RN7SL261P, LOC105371235, 103 more genes
    nsv5200303copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,818,702-149,378,266 , GRCh38.p12 chr7: 58,093,723-62,429,627 , GRCh38.p12 chr1: 144,536,526-148,549,211 , LOC105371254, 151 more genes
    nsv5161924mobile element insertion1nstd203human GRCh38 chr1: 147,643,818-147,643,833 , GRCh37.p13 chr1|NW_003871055.3: 4,459,231-4,459,246 , GRCh37.p13 chr1: 147,115,618-147,115,633 ACP6
    nsv5076937mobile element insertion1nstd203human GRCh38 chr1: 147,653,213-147,653,224 , GRCh37.p13 chr1|NW_003871055.3: 4,468,626-4,468,637 ACP6
    nsv5076070mobile element insertion1nstd203human GRCh38 chr1: 147,653,165-147,653,211 , GRCh37.p13 chr1|NW_003871055.3: 4,468,578-4,468,624 ACP6
    nsv5073413mobile element insertion1nstd203human GRCh38 chr1: 147,652,844-147,652,889 , GRCh37.p13 chr1: 147,124,651-147,124,696 , GRCh37.p13 chr1|NW_003871055.3: 4,468,257-4,468,302 ACP6
    nsv5069888mobile element insertion1nstd203human GRCh38 chr1: 147,653,211-147,653,244 , GRCh37.p13 chr1|NW_003871055.3: 4,468,624-4,468,657 ACP6
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