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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5882916copy number variation1nstd209human GRCh38 chrX: 65,772,967-65,773,070 , GRCh37.p13 chrX: 64,992,809-64,992,912 NANOGP9
    nsv5666225copy number variation1nstd207human GRCh38 chrX: 65,771,023-65,771,112 , GRCh37.p13 chrX: 64,990,865-64,990,954 NANOGP9
    nsv5617037insertion1nstd207human GRCh38 chrX: 65,772,967-65,772,967 , GRCh37.p13 chrX: 64,992,809-64,992,809 NANOGP9
    nsv5610683insertion1nstd207human GRCh38 chrX: 65,770,998-65,770,998 , GRCh37.p13 chrX: 64,990,840-64,990,840 NANOGP9
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5424016copy number variation1nstd206human GRCh38 chrX: 65,770,999-65,771,146 , GRCh37.p13 chrX: 64,990,841-64,990,988 NANOGP9
    nsv5419594copy number variation1nstd206human GRCh38 chrX: 65,771,040-65,771,097 , GRCh37.p13 chrX: 64,990,882-64,990,939 NANOGP9
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5384849copy number variation1nstd186human GRCh37 chrX: 64,992,809-64,992,923 , GRCh38.p12 chrX: 65,772,967-65,773,081 NANOGP9
    nsv5376384translocation1nstd200human GRCh38 chrX: 65,771,748-65,771,748 , GRCh38 chrX: 65,771,685-65,771,685 , GRCh37.p13 chrX: 64,991,527-64,991,527 , GRCh37.p13 chrX: 64,991,590-64,991,590 NANOGP9
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4909056copy number variation1nstd200human GRCh38 chrX: 65,710,543-68,026,703 , GRCh37.p13 chrX: 64,930,405-67,246,545 AR, NXTAR, 19 more genes
    nsv4782076copy number variation1nstd200human GRCh37 chrX: 64,992,809-64,992,923 , GRCh38.p12 chrX: 65,772,967-65,773,081 NANOGP9
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4746008insertion1nstd199human GRCh37 chrX: 64,990,900-64,990,900 , GRCh38.p12 chrX: 65,771,058-65,771,058 NANOGP9
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4703649copy number variation1nstd195human GRCh37 chrX: 64,840,101-65,053,701 , GRCh38.p12 chrX: 65,620,222-65,833,859 MSN, NANOGP9, 2 more genes
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 more genes
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