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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2661219copy number variation458estd199human GRCh37 chr8: 48,180,445-48,214,692 , GRCh38.p12 chr8: 47,276,396-47,302,103 SPIDR
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2656701copy number variation437estd199human GRCh37 chr16: 78,371,638-78,384,898 , GRCh38.p12 chr16: 78,337,741-78,351,001 WWOX
    esv2672086copy number variation8estd199human GRCh37 chr2: 55,323,854-55,336,822 , GRCh38.p12 chr2: 55,096,718-55,109,686 RTN4
    esv2659892copy number variation75estd199human GRCh37 chr3: 114,656,245-114,668,792 , GRCh38.p12 chr3: 114,937,398-114,949,945 ZBTB20
    esv2670596copy number variation22estd199human GRCh37 chr4: 151,874,295-151,885,892 , GRCh38.p12 chr4: 150,953,143-150,964,740 LRBA
    esv2677682copy number variation11estd199human GRCh37 chr17: 77,989,745-78,000,992 , GRCh38.p12 chr17: 80,015,946-80,027,193 TBC1D16
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2657260copy number variation826estd199human GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083 LINC01943
    esv2658229copy number variation46estd199human GRCh37 chr3: 125,712,244-125,722,069 , GRCh38.p12 chr3: 125,993,401-126,003,226 ALG1L1P
    esv2666144copy number variation73estd199human GRCh37 chr17: 77,992,012-78,000,841 , GRCh38.p12 chr17: 80,018,213-80,027,042 TBC1D16
    esv2660064copy number variation10estd199human GRCh37 chr4: 15,760,385-15,768,830 , GRCh38.p12 chr4: 15,758,762-15,767,207 BST1
    esv2657053copy number variation4estd199human GRCh37 chr2: 131,639,036-131,647,339 , GRCh38.p12 chr2: 130,881,463-130,889,766 ARHGEF4
    esv2677767copy number variation161estd199human GRCh37 chr4: 21,369,090-21,376,907 , GRCh38.p12 chr4: 21,367,467-21,375,284 KCNIP4
    esv2662072copy number variation185estd199human GRCh37 chr3: 193,135,464-193,142,943 , GRCh38.p12 chr3: 193,417,675-193,425,154 ATP13A4
    esv2668452copy number variation609estd199human GRCh37 chr6: 165,724,666-165,732,132 , GRCh38.p12 chr6: 165,311,177-165,318,643 LOC105378113
    esv2678795copy number variation16estd199human GRCh37 chr5: 17,463,660-17,471,088 , GRCh38.p12 chr5: 17,463,551-17,470,979 LINC02218
    esv2671970copy number variation109estd199human GRCh37 chr19: 54,555,086-54,562,386 , GRCh38.p12 chr19|NW_003571061.2: 26,199-33,499 , GRCh38.p12 chr19|NW_003571057.2: 26,199-33,499 , GRCh38.p12 chr19|NW_003571058.2: 26,199-33,499 , GRCh38.p12 chr19|NW_003571059.2: 26,199-33,499 , GRCh38.p12 chr19|NW_003571060.1: 26,199-33,499 , GRCh38.p12 chr19|NW_003571056.2: 26,199-33,499 , GRCh38.p12 chr19|NW_003571055.2: 26,199-33,499 , GRCh38.p12 chr19|NW_003571054.1: 26,199-33,499 , GRCh38.p12 chr19: 54,051,832-54,059,132 , GRCh38.p12 chr19|NT_187693.1: 26,199-33,499 VSTM1
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