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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
    nsv5867832copy number variation1nstd209human GRCh38 chr1: 148,012,263-148,158,531 , GRCh37.p13 chr1|NW_003871055.3: 4,827,676-4,973,944 , RNU1-129P, 9 more genes
    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
    nsv5433871copy number variation1nstd206human GRCh38 chr1: 148,030,587-148,036,793 , GRCh37.p13 chr1|NW_003871055.3: 4,846,000-4,852,206 RNVU1-7, TRQ-CTG3-2
    nsv5433167copy number variation1nstd206human GRCh38 chr1: 148,012,226-148,158,542 , GRCh37.p13 chr1|NW_003871055.3: 4,827,639-4,973,955 , NBPF11, 9 more genes
    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
    nsv5219313copy number variation1nstd204human GRCh38.p13 chr1: 148,037,374-148,038,767 , GRCh37.p13 chr1|NW_003871055.3: 4,852,787-4,854,180 RNVU1-7
    nsv5218834copy number variation1nstd204human GRCh38.p13 chr1: 148,033,001-148,042,600 , GRCh37.p13 chr1|NW_003871055.3: 4,848,414-4,858,013 RNVU1-7, TRQ-CTG3-2
    nsv5217125copy number variation1nstd204human GRCh38.p13 chr1: 148,037,301-148,037,900 , GRCh37.p13 chr1|NW_003871055.3: 4,852,714-4,853,313 RNVU1-7
    nsv5213228copy number variation1nstd204human GRCh38.p13 chr1: 148,038,501-148,045,800 , GRCh37.p13 chr1|NW_003871055.3: 4,853,914-4,861,213 RNVU1-7
    nsv5210051copy number variation1nstd204human GRCh37.p13 chr1|NW_003871055.3: 4,827,614-4,885,913 , GRCh38.p13 chr1: 148,012,201-148,070,500 , RNVU1-7, 5 more genes
    nsv5209898copy number variation1nstd204human GRCh38.p13 chr1: 148,036,001-148,037,900 , GRCh37.p13 chr1|NW_003871055.3: 4,851,414-4,853,313 RNVU1-7
    nsv5208244copy number variation1nstd204human GRCh38.p13 chr1: 148,037,274-148,039,624 , GRCh37.p13 chr1|NW_003871055.3: 4,852,687-4,855,037 RNVU1-7
    nsv5205587copy number variation1nstd204human GRCh38.p13 chr1: 148,031,101-148,039,000 , GRCh37.p13 chr1|NW_003871055.3: 4,846,514-4,854,413 TRQ-CTG3-2, RNVU1-7
    nsv5203193copy number variation1nstd204human GRCh38.p13 chr1: 148,037,301-148,042,400 , GRCh37.p13 chr1|NW_003871055.3: 4,852,714-4,857,813 RNVU1-7
    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
    nsv5200997copy number variation1nstd204human GRCh38.p13 chr1: 148,029,701-148,042,600 , GRCh37.p13 chr1|NW_003871055.3: 4,845,114-4,858,013 TRQ-CTG3-2, RNVU1-7
    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
    nsv4897289copy number variation1nstd200human GRCh38 chr1: 148,034,503-148,127,826 , GRCh37.p13 chr1|NW_003871055.3: 4,849,916-4,943,239 TRN-GTT9-2, PFN1P4, 3 more genes
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