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Items: 1 to 20 of 1111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2673642copy number variation50estd199human GRCh37 chrX: 91,853,345-91,909,992 , GRCh38.p12 chrX: 92,598,346-92,654,993 PCDH11X
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2664197copy number variation34estd199human GRCh37 chr11: 7,809,445-7,834,142 , GRCh38.p12 chr11: 7,787,898-7,812,595 , GRCh38.p12 chr11|NT_187583.1: 8,766-33,463 , GRCh38.p12 chr11|NW_011332695.1: 8,766-33,465 OR5P2
    esv2671157copy number variation55estd199human GRCh37 chr6: 78,879,858-78,898,877 , GRCh38.p12 chr6: 78,170,141-78,189,160 LOC105377865
    esv2662905copy number variation26estd199human GRCh37 chr6: 78,879,858-78,898,877 , GRCh38.p12 chr6: 78,170,141-78,189,160 LOC105377865
    esv2669049copy number variation26estd199human GRCh37 chr2: 203,295,345-203,313,492 , GRCh38.p12 chr2: 202,430,622-202,448,769 BMPR2
    esv2659014copy number variation1estd199human GRCh37 chr9: 73,501,078-73,514,631 , GRCh38.p12 chr9: 70,886,162-70,899,715 TRPM3
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2668652copy number variation25estd199human GRCh37 chr1: 111,377,295-111,389,642 , GRCh38.p12 chr1: 110,834,673-110,847,020 NRBF2P3
    esv2664803copy number variation436estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2665413copy number variation30estd199human GRCh37 chr8: 63,214,945-63,226,892 , GRCh38.p12 chr8: 62,302,386-62,314,333 NKAIN3
    esv2670295copy number variation118estd199human GRCh37 chr3: 114,656,952-114,668,601 , GRCh38.p12 chr3: 114,938,105-114,949,754 ZBTB20
    esv2674298copy number variation219estd199human GRCh37 chr1: 35,101,421-35,111,976 , GRCh38.p12 chr1: 34,635,820-34,646,375 LOC105378641
    esv2660593copy number variation56estd199human GRCh37 chrX: 91,610,345-91,620,792 , GRCh38.p12 chrX: 92,355,346-92,365,793 PCDH11X
    esv2672284copy number variation80estd199human GRCh37 chr11: 107,233,995-107,244,392 , GRCh38.p12 chr11: 107,363,269-107,373,666 CWF19L2
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2658946copy number variation162estd199human GRCh37 chr10: 96,867,192-96,874,942 , GRCh38.p12 chr10: 95,107,435-95,115,185
    esv2657498copy number variation116estd199human GRCh37 chr4: 21,160,045-21,167,592 , GRCh38.p12 chr4: 21,158,422-21,165,969 KCNIP4
    esv2668452copy number variation609estd199human GRCh37 chr6: 165,724,666-165,732,132 , GRCh38.p12 chr6: 165,311,177-165,318,643 LOC105378113
    esv2669295copy number variation13estd199human GRCh37 chr2: 125,651,791-125,659,029 , GRCh38.p12 chr2: 124,894,214-124,901,452 CNTNAP5
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