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Items: 1 to 20 of 292

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125132insertion1nstd186human GRCh37 chrX: 84,009,827-84,009,827 , GRCh38.p12 chrX: 84,754,819-84,754,819 SETP4, TEX16P
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5973716copy number variation1nstd209human GRCh38 chrX: 84,749,354-84,756,553 , GRCh37.p13 chrX: 84,004,362-84,011,561 SETP4, TEX16P
    nsv5955998insertion1nstd209human GRCh38 chrX: 84,754,819-84,754,819 , GRCh37.p13 chrX: 84,009,827-84,009,827 SETP4, TEX16P
    nsv5882611copy number variation1nstd209human GRCh38 chrX: 84,749,687-84,756,504 , GRCh37.p13 chrX: 84,004,695-84,011,512 TEX16P, SETP4
    nsv5670004copy number variation1nstd207human GRCh38 chrX: 84,749,687-84,756,504 , GRCh37.p13 chrX: 84,004,695-84,011,512 TEX16P, SETP4
    nsv5613401insertion1nstd207human GRCh38 chrX: 84,754,819-84,754,819 , GRCh37.p13 chrX: 84,009,827-84,009,827 TEX16P, SETP4
    nsv5542518insertion1nstd206human GRCh38 chrX: 84,754,819-84,754,819 , GRCh37.p13 chrX: 84,009,827-84,009,827 SETP4, TEX16P
    nsv5422664copy number variation1nstd206human GRCh38 chrX: 84,749,690-84,756,505 , GRCh37.p13 chrX: 84,004,698-84,011,513 SETP4, TEX16P
    nsv5417717copy number variation1nstd206human GRCh38 chrX: 84,754,987-84,755,603 , GRCh37.p13 chrX: 84,009,995-84,010,611 TEX16P, SETP4
    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
    nsv4771713copy number variation1nstd200human GRCh37 chrX: 84,004,698-84,011,513 , GRCh38.p12 chrX: 84,749,690-84,756,505 TEX16P, SETP4
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4749027insertion1nstd199human GRCh37 chrX: 84,009,821-84,009,821 , GRCh38.p12 chrX: 84,754,813-84,754,813 SETP4, TEX16P
    nsv4728601copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,514,079-127,770,854 , GRCh38.p12 chrX: 78,258,582-128,636,876 PHB1P10, SNORA35, 565 more genes
    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
    nsv4709531translocation1nstd195human GRCh37 chrX: 84,010,381-84,010,381 , GRCh38.p12 chrX: 84,755,373-84,755,373 , GRCh37 chr5: 96,392,766-96,392,766 , GRCh38.p12 chr5: 97,057,062-97,057,062 SETP22, SETP4, 1 more genes
    nsv4703799translocation1nstd195human GRCh37 chrX: 84,010,380-84,010,380 , GRCh38.p12 chrX: 84,755,372-84,755,372 , GRCh37 chr5: 96,392,766-96,392,766 , GRCh38.p12 chr5: 97,057,062-97,057,062 SETP22, SETP4, 1 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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