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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5369192translocation1nstd200human GRCh38 chr6: 6,208,123-6,208,123 , GRCh38 chr6: 6,168,841-6,168,841 , GRCh37.p13 chr6: 6,169,074-6,169,074 , GRCh37.p13 chr6: 6,208,356-6,208,356 F13A1, MIR5683, 1 more genes
    nsv5340654translocation1nstd200human GRCh37 chr6: 6,208,356-6,208,356 , GRCh37 chr6: 6,169,074-6,169,074 , GRCh38.p12 chr6: 6,208,123-6,208,123 , GRCh38.p12 chr6: 6,168,841-6,168,841 F13A1, MIR5683, 1 more genes
    nsv4947546copy number variation1nstd200human GRCh38 chr6: 6,147,324-6,182,328 , GRCh37.p13 chr6: 6,147,557-6,182,561 F13A1, MIR5683, 1 more genes
    nsv4809544copy number variation1nstd200human GRCh37 chr6: 6,147,557-6,182,561 , GRCh38.p12 chr6: 6,147,324-6,182,328 MIR7853, MIR5683, 1 more genes
    nsv4675053copy number variation1nstd102humanPathogenic GRCh37 chr6: 5,997,521-8,570,039 , GRCh38.p12 chr6: 5,997,288-8,569,806 BTF3P7, EEF1E1, 42 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv3923898copy number variation1nstd102humanUncertain significance NCBI36 chr6: 6,112,372-6,250,566 , GRCh37.p13 chr6: 6,167,373-6,305,567 , GRCh38.p12 chr6: 6,167,140-6,305,334 MIR7853, MIR5683, 1 more genes
    nsv3923249copy number variation1nstd102humanPathogenic NCBI36 chr6: 110,675-8,981,266 , GRCh38 chr6: 165,675-9,036,034 , GRCh37 chr6: 165,675-9,036,267 LOC100506207, LOC105374889, 148 more genes
    nsv3922576copy number variation1nstd102humanPathogenic GRCh37 chr6: 164,633-6,284,470 , GRCh38 chr6: 164,633-6,284,237 , NCBI36 chr6: 109,633-6,229,469 GLRX3P2, CDYL, 106 more genes
    nsv3922052copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414 ECI2-DT, RNU1-11P, 268 more genes
    nsv3921817copy number variation1nstd102humanPathogenic GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998 RN7SKP293, LOC105374906, 230 more genes
    nsv3921027copy number variation1nstd102humanPathogenic GRCh38 chr6: 389,423-13,474,956 , GRCh37 chr6: 389,423-13,475,188 , NCBI36 chr6: 334,423-13,583,167 LOC105374898, HIVEP1, 215 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3919014copy number variation1nstd102humanPathogenic GRCh38 chr6: 4,427,090-8,391,140 , NCBI36 chr6: 4,372,323-8,336,372 , GRCh37 chr6: 4,427,324-8,391,373 RREB1, FARS2, 65 more genes
    nsv3918645copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 101,974-11,659,036 , GRCh37 chr6: 156,974-11,551,050 , GRCh38 chr6: 156,974-11,550,817 BMP6, BPHL, 194 more genes
    nsv3916794copy number variation1nstd102humanUncertain significance NCBI36 chr6: 6,112,372-6,274,325 , GRCh37.p13 chr6: 6,167,373-6,329,326 , GRCh38.p12 chr6: 6,167,140-6,329,093 MIR5683, F13A1, 1 more genes
    nsv3916436copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-7,122,992 , NCBI36 chr6: 101,974-7,067,991 , GRCh38 chr6: 156,974-7,122,759 LINC01011, FOXF2, 119 more genes
    nsv3914672copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 101,974-13,189,419 , GRCh37 chr6: 156,974-13,081,433 , GRCh38 chr6: 156,974-13,081,201 BMP6, BPHL, 212 more genes
    nsv3914400copy number variation1nstd102humanPathogenic NCBI36 chr6: 97,634-6,235,036 , GRCh38 chr6: 152,634-6,289,804 , GRCh37 chr6: 152,634-6,290,037 LOC105374898, SERPINB9-AS1, 106 more genes
    nsv3914068copy number variation1nstd102humanPathogenic NCBI36 chr6: 4,014,025-13,376,010 , GRCh38 chr6: 4,068,792-13,267,799 , GRCh37 chr6: 4,069,026-13,268,031 SSR1, LOC107986560, 145 more genes
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