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Items: 1 to 20 of 263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099179copy number variation1nstd231human GRCh38.p12 chr1: 16,321,557-16,480,717 , GRCh37 chr1: 16,648,052-16,807,212 SZRD1, FBXO42, 5 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7056505inversion1nstd229human GRCh38 chr1: 16,154,147-16,435,510 , GRCh37.p13 chr1: 16,480,642-16,762,005 EPHA2-AS1, SZRD1, 8 more genes
    nsv7053250inversion1nstd229human GRCh38 chr1: 16,399,708-16,517,073 , GRCh37.p13 chr1: 16,726,203-16,843,568 SPATA21, RNU1-1, 3 more genes
    nsv7049927inversion1nstd229human GRCh38 chr1: 12,447,483-21,286,051 , GRCh37.p13 chr1: 12,507,539-21,612,544 SLC25A34, RNA5SP41, 238 more genes
    nsv6643806copy number variation1nstd229human GRCh38 chr1: 16,394,681-16,394,706 , GRCh37.p13 chr1: 16,721,176-16,721,201 SPATA21, SZRD1
    nsv6643795copy number variation1nstd229human GRCh38 chr1: 16,376,372-16,400,781 , GRCh37.p13 chr1: 16,702,867-16,727,276 SZRD1, SPATA21
    nsv6643699copy number variation1nstd229human GRCh38 chr1: 16,432,750-16,436,695 , GRCh37.p13 chr1: 16,759,245-16,763,190 SPATA21
    nsv6643696copy number variation1nstd229human GRCh38 chr1: 16,424,691-16,428,624 , GRCh37.p13 chr1: 16,751,186-16,755,119 SPATA21
    nsv6643681copy number variation1nstd229human GRCh38 chr1: 16,377,901-16,419,600 , GRCh37.p13 chr1: 16,704,396-16,746,095 SZRD1, SPATA21
    nsv6643456copy number variation1nstd229human GRCh38 chr1: 16,407,485-16,411,052 , GRCh37.p13 chr1: 16,733,980-16,737,547 SPATA21
    nsv6643455copy number variation1nstd229human GRCh38 chr1: 16,401,155-16,412,250 , GRCh37.p13 chr1: 16,727,650-16,738,745 SPATA21
    nsv6636785copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276 GPR157, MST1L, 313 more genes
    nsv6625669copy number variation2nstd224human GRCh37 chr1: 16,722,692-16,794,254 , GRCh38.p12 chr1: 16,396,197-16,467,759 NECAP2, LINC01772, 3 more genes
    nsv6555084inversion1nstd223human GRCh38 chr1: 16,423,413-16,423,732 , GRCh37.p13 chr1: 16,749,908-16,750,227 SPATA21
    nsv6551943inversion1nstd223human GRCh38 chr1: 16,435,452-16,436,163 , GRCh37.p13 chr1: 16,761,947-16,762,658 SPATA21
    nsv6539413inversion1nstd223human GRCh38 chr1: 16,429,578-16,430,228 , GRCh37.p13 chr1: 16,756,073-16,756,723 SPATA21
    nsv6333479copy number variation1nstd223human GRCh38 chr1: 16,429,577-16,453,212 , GRCh37.p13 chr1: 16,756,072-16,779,707 NECAP2, SPATA21
    nsv6332761copy number variation1nstd223human GRCh38 chr1: 16,410,663-16,412,715 , GRCh37.p13 chr1: 16,737,158-16,739,210 SPATA21
    nsv6325543copy number variation1nstd223human GRCh38 chr1: 16,408,869-16,430,120 , GRCh37.p13 chr1: 16,735,364-16,756,615 SPATA21
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