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Items: 1 to 20 of 1317

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047747inversion1nstd229human GRCh38 chr1: 169,294,027-169,294,051 , GRCh37.p13 chr1: 169,263,265-169,263,289 NME7
    nsv6644466copy number variation1nstd229human GRCh38 chr1: 169,285,165-169,285,388 , GRCh37.p13 chr1: 169,254,403-169,254,626 NME7
    nsv6644465copy number variation1nstd229human GRCh38 chr1: 169,282,980-169,437,910 , GRCh37.p13 chr1: 169,252,218-169,407,148 CCDC181, BLZF1, 1 more genes
    nsv6644464copy number variation1nstd229human GRCh38 chr1: 169,278,706-169,386,194 , GRCh37.p13 chr1: 169,247,944-169,355,432 BLZF1, NME7
    nsv6644400copy number variation1nstd229human GRCh38 chr1: 169,319,124-169,329,332 , GRCh37.p13 chr1: 169,288,362-169,298,570 NME7
    nsv6644399copy number variation1nstd229human GRCh38 chr1: 169,298,244-169,328,804 , GRCh37.p13 chr1: 169,267,482-169,298,042 NME7
    nsv6644398copy number variation1nstd229human GRCh38 chr1: 169,190,782-169,191,111 , GRCh37.p13 chr1: 169,160,020-169,160,349 NME7
    nsv6644397copy number variation1nstd229human GRCh38 chr1: 169,183,347-169,210,503 , GRCh37.p13 chr1: 169,152,585-169,179,741 NME7
    nsv6644396copy number variation1nstd229human GRCh38 chr1: 169,174,001-169,178,900 , GRCh37.p13 chr1: 169,143,239-169,148,138 NME7
    nsv6644297copy number variation1nstd229human GRCh38 chr1: 169,337,783-169,372,210 , GRCh37.p13 chr1: 169,307,021-169,341,448 BLZF1, NME7
    nsv6644296copy number variation1nstd229human GRCh38 chr1: 169,334,479-169,358,927 , GRCh37.p13 chr1: 169,303,717-169,328,165 NME7
    nsv6644295copy number variation1nstd229human GRCh38 chr1: 169,306,951-169,309,729 , GRCh37.p13 chr1: 169,276,189-169,278,967 NME7
    nsv6644294copy number variation1nstd229human GRCh38 chr1: 169,306,397-169,323,069 , GRCh37.p13 chr1: 169,275,635-169,292,307 NME7
    nsv6644292copy number variation1nstd229human GRCh38 chr1: 169,255,701-169,282,600 , GRCh37.p13 chr1: 169,224,939-169,251,838 NME7
    nsv6644291copy number variation1nstd229human GRCh38 chr1: 169,231,633-169,231,992 , GRCh37.p13 chr1: 169,200,871-169,201,230 NME7
    nsv6644289copy number variation1nstd229human GRCh38 chr1: 169,145,278-169,163,562 , GRCh37.p13 chr1: 169,114,516-169,132,800 NME7
    nsv6644256copy number variation1nstd229human GRCh38 chr1: 168,110,598-170,953,728 , GRCh37.p13 chr1: 168,079,836-170,922,869 SELL, RPL7AP21, 55 more genes
    nsv6644028copy number variation1nstd229human GRCh38 chr1: 169,276,738-169,314,347 , GRCh37.p13 chr1: 169,245,976-169,283,585 NME7
    nsv6644026copy number variation1nstd229human GRCh38 chr1: 169,236,172-169,240,728 , GRCh37.p13 chr1: 169,205,410-169,209,966 NME7
    nsv6644025copy number variation1nstd229human GRCh38 chr1: 169,223,901-169,226,700 , GRCh37.p13 chr1: 169,193,139-169,195,938 NME7
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