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Items: 1 to 20 of 1141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2676068copy number variation152estd199human GRCh37 chr6: 32,454,245-32,511,792 , GRCh38.p12 chr6: 32,486,468-32,544,015 HLA-DRB5
    esv2664200copy number variation92estd199human GRCh37 chr4: 75,282,645-75,323,192 , GRCh38.p12 chr4: 74,416,928-74,457,475 AREG
    esv2660522copy number variation236estd199human GRCh37 chr1: 207,700,012-207,737,123 , GRCh38.p12 chr1: 207,526,667-207,563,778 CR1
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2666578copy number variation167estd199human GRCh37 chr17: 77,462,245-77,494,392 , GRCh38.p12 chr17: 79,466,163-79,498,310 RBFOX3
    esv2661219copy number variation458estd199human GRCh37 chr8: 48,180,445-48,214,692 , GRCh38.p12 chr8: 47,276,396-47,302,103 SPIDR
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2659504copy number variation6estd199human GRCh37 chr5: 41,226,813-41,243,961 , GRCh38.p12 chr5: 41,226,711-41,243,859 C6
    esv2670760copy number variation36estd199human GRCh37 chr7: 100,326,395-100,343,242 , GRCh38.p12 chr7: 100,728,772-100,745,619 ZAN
    esv2662901copy number variation324estd199human GRCh37 chr9: 41,969,445-41,984,392 , GRCh38.p12 chr9: 39,824,427-39,839,374 FGF7P3
    esv2667042copy number variation3estd199human GRCh37 chrX: 130,778,582-130,793,458 , GRCh38.p12 chrX: 131,644,579-131,659,445 HDGFP1
    esv2662537copy number variation71estd199human GRCh37 chr3: 75,567,345-75,581,692 , GRCh38.p12 chr3: 75,518,194-75,532,541 SNRPCP10
    esv2661760copy number variation42estd199human GRCh37 chr7: 62,965,045-62,979,392 , GRCh38.p12 chr7: 63,504,667-63,519,014 PHKG1P2
    esv2663062copy number variation52estd199human GRCh37 chr7: 155,594,945-155,608,992 , GRCh38.p12 chr7: 155,802,251-155,816,298 SHH
    esv2675982copy number variation92estd199human GRCh37 chr8: 21,624,845-21,638,692 , GRCh38.p12 chr8: 21,767,333-21,781,180 GFRA2
    esv2669985copy number variation97estd199human GRCh37 chr19: 1,852,045-1,864,992 , GRCh38.p12 chr19: 1,852,046-1,864,993 KLF16
    esv2659442copy number variation87estd199human GRCh37 chr7: 150,945-159,992 , GRCh38.p12 chr7: 150,945-159,992 , GRCh38.p12 chr7|NT_187558.1: 106,750-119,335 , GRCh38.p12 chr7|NT_187653.1: 143,266-152,313 LINC03014
    esv2665606copy number variation90estd199human GRCh37 chr7: 91,031,083-91,042,584 , GRCh38.p12 chr7: 91,401,768-91,413,269 LINC02932
    esv2670618copy number variation111estd199human GRCh37 chr11: 89,495,739-89,507,199 , GRCh38.p12 chr11: 89,762,571-89,774,031 TRIM49
    esv2663832copy number variation109estd199human GRCh37 chr4: 118,579,966-118,591,119 , GRCh38.p12 chr4: 117,658,811-117,669,964 LINC01378
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