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Items: 1 to 20 of 937

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148054copy number variation1nstd102humanPathogenic GRCh37 chr1: 142,535,935-157,648,813 , GRCh38.p12 chr1: 120,175,847-149,601,750 , TRN-GTT12-1, 266 more genes
    nsv7141422insertion1nstd232human GRCh37.p13 chr1: 145,026,745-145,026,745 , GRCh38.p12 chr1: 148,857,669-148,857,669 PDE4DIP, LOC112268272
    nsv7099227copy number variation1nstd231human GRCh37 chr1: 144,849,458-144,956,561 , GRCh38.p12 chr1: 148,927,928-149,034,985 PDE4DIP, RNU2-38P
    nsv7098839copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,405,854-147,597,284 , GRCh38.p12 chr1: 145,598,009-149,077,123 CCT8P1, LINC01719, 120 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7051656inversion1nstd229human GRCh37.p13 chr1|NW_003871055.3: 5,745,861-6,015,183 , GRCh38 chr1: 148,930,448-149,199,770 , GRCh37.p13 chr1: 144,577,358-144,954,041 PDE4DIP, NBPF9, 6 more genes
    nsv7038936inversion1nstd229human GRCh37.p13 chr1|NW_003871055.3: 5,745,916-6,015,189 , GRCh38 chr1: 148,930,503-149,199,776 , GRCh37.p13 chr1: 144,577,358-144,953,986 LOC653513, LOC102723348, 6 more genes
    nsv6634349copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,157,447-148,016,122 , GRCh38.p12 chr1: 144,536,526-149,492,442 , TRN-GTT10-1, 170 more genes
    nsv6634346copy number variation1nstd102humanPathogenic GRCh37 chr1: 144,893,419-144,937,891 , GRCh38.p12 chr1: 148,946,598-148,991,055 PDE4DIP
    nsv6625826copy number variation1nstd224human GRCh37 chr1: 144,816,621-144,876,030 , GRCh38.p12 chr1: 149,008,442-149,059,736 PDE4DIP, NBPF9
    nsv6625631copy number variation1nstd224human GRCh37 chr1: 144,994,670-145,075,809 , GRCh38.p12 chr1: 148,808,558-148,889,815 PDE4DIP, RN7SKP88, 1 more genes
    nsv6625630copy number variation1nstd224human GRCh37 chr1: 144,850,564-144,906,508 , GRCh38.p12 chr1: 148,977,966-149,033,879 PDE4DIP
    nsv6542731inversion1nstd223human GRCh38 chr1: 147,056,374-148,969,054 , GRCh37.p13 chr1|NW_003871055.3: 3,871,787-5,784,467 , LINC01731, 75 more genes
    nsv6334908copy number variation1nstd223human GRCh38 chr1: 149,021,001-149,023,300 , GRCh37.p13 chr1: 144,861,171-144,863,470 , GRCh37.p13 chr1|NW_003871055.3: 5,836,414-5,838,713 PDE4DIP
    nsv6325717copy number variation1nstd223human GRCh38 chr1: 148,974,101-149,005,300 , GRCh37.p13 chr1: 144,879,172-144,910,373 , GRCh37.p13 chr1|NW_003871055.3: 5,789,514-5,820,713 PDE4DIP
    nsv6324165copy number variation1nstd223human GRCh38 chr1: 148,959,801-148,960,700 , GRCh37.p13 chr1: 144,923,775-144,924,688 , GRCh37.p13 chr1|NW_003871055.3: 5,775,214-5,776,113 PDE4DIP
    nsv6319828copy number variation1nstd223human GRCh38 chr1: 148,823,201-148,824,700 , GRCh37.p13 chr1: 145,059,681-145,061,179 , GRCh37.p13 chr1|NW_003871055.3: 5,638,614-5,640,113 PDE4DIP
    nsv6296847copy number variation1nstd186human GRCh37 chr1: 145,069,807-145,079,779 , GRCh38.p12 chr1: 148,804,587-148,814,587 PDE4DIP
    nsv6295365copy number variation1nstd186human GRCh37 chr1: 144,860,675-144,860,823 , GRCh38.p12 chr1: 149,023,648-149,023,768 PDE4DIP
    nsv6290073copy number variation1nstd218human GRCh38.p12 chr1: 143,511,409-149,082,254 , GRCh37 chr1: 147,824,148-149,378,266 , BCL9, 215 more genes
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