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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2737658copy number variation37estd201human GRCh37 chr8: 137,680,474-137,862,283 , GRCh38.p12 chr8: 136,668,231-136,850,040 LINC02055
    esv2745334copy number variation162estd201human GRCh37 chr11: 134,354,170-134,474,375 , GRCh38.p12 chr11: 134,484,276-134,604,481 B3GAT1-DT
    esv2745085copy number variation1estd201human GRCh37 chr11: 112,951,570-113,025,434 , GRCh38.p12 chr11: 113,080,848-113,154,712 NCAM1
    esv2714071copy number variation19estd201human GRCh37 chr16: 22,019,718-22,086,803 , GRCh38.p12 chr16: 22,008,397-22,075,482 , GRCh38.p12 chr16|NW_017852933.1: 1,029,556-1,096,641 MOSMO
    esv2733876copy number variation75estd201human GRCh37 chr7: 3,708,209-3,765,709 , GRCh38.p12 chr7: 3,668,577-3,726,077 SDK1
    esv2733915copy number variation28estd201human GRCh37 chr7: 5,795,550-5,852,483 , GRCh38.p12 chr7: 5,755,919-5,812,852 RNF216
    esv2720361copy number variation324estd201human GRCh37 chr1: 2,583,966-2,628,877 , GRCh38.p12 chr1|NT_187515.1: 219,010-258,013 , GRCh38.p12 chr1: 2,652,527-2,697,438 TTC34
    esv2720584copy number variation301estd201human GRCh37 chr1: 2,583,971-2,628,877 , GRCh38.p12 chr1|NT_187515.1: 219,010-258,013 , GRCh38.p12 chr1: 2,652,532-2,697,438 TTC34
    esv2720806copy number variation265estd201human GRCh37 chr1: 2,584,075-2,628,877 , GRCh38.p12 chr1|NT_187515.1: 219,010-258,013 , GRCh38.p12 chr1: 2,652,636-2,697,438 TTC34
    esv2721028copy number variation255estd201human GRCh37 chr1: 2,584,101-2,628,877 , GRCh38.p12 chr1: 2,652,662-2,697,438 , GRCh38.p12 chr1|NT_187515.1: 219,010-258,013 TTC34
    esv2720139copy number variation274estd201human GRCh37 chr1: 2,583,492-2,620,302 , GRCh38.p12 chr1|NT_187515.1: 219,010-249,438 , GRCh38.p12 chr1: 2,652,053-2,688,863 TTC34
    esv2735255copy number variation70estd201human GRCh37 chr7: 141,751,744-141,786,850 , GRCh38.p12 chr7: 142,051,944-142,087,050 , GRCh38.p12 chr7|NT_187562.1: 13,824-48,930 MGAM
    esv2721361copy number variation92estd201human GRCh37 chr1: 2,586,526-2,620,302 , GRCh38.p12 chr1: 2,655,087-2,688,863 , GRCh38.p12 chr1|NT_187515.1: 219,010-249,438 TTC34
    esv2722072copy number variation80estd201human GRCh37 chr20: 1,561,011-1,594,167 , GRCh38.p12 chr20: 1,580,365-1,613,521 SIRPB1
    esv2744176copy number variation107estd201human GRCh37 chr11: 18,957,902-18,986,343 , GRCh38.p12 chr11: 18,936,355-18,964,796 MRGPRX11P
    esv2721472copy number variation72estd201human GRCh37 chr1: 2,603,375-2,628,704 , GRCh38.p12 chr1: 2,671,936-2,697,265 TTC34
    esv2744174copy number variation18estd201human GRCh37 chr11: 18,941,665-18,963,824 , GRCh38.p12 chr11: 18,920,118-18,942,277 MRGPRX1
    esv2743978copy number variation96estd201human GRCh37 chr11: 1,915,287-1,936,956 , GRCh38.p12 chr11: 1,894,057-1,915,726 LINC01150
    esv2716009copy number variation90estd201human GRCh37 chr17: 45,249,418-45,266,454 , GRCh38.p12 chr17: 47,172,052-47,189,088 CDC27
    esv2718556copy number variation5estd201human GRCh37 chr19: 40,369,136-40,385,544 , GRCh38.p12 chr19: 39,878,496-39,894,904 , GRCh38.p12 chr19|NW_009646206.1: 138,372-154,780 FCGBP
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