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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5893304copy number variation1nstd209human GRCh38 chr6: 29,833,095-30,011,611 , GRCh37.p13 chr6: 29,800,872-29,979,388 DDX39BP1, HCG4P5, 24 more genes
    nsv4940630copy number variation1nstd200human GRCh38 chr6: 29,995,197-30,020,159 , GRCh37.p13 chr6: 29,962,974-29,987,936 MCCD1P2, HLA-J, 3 more genes
    nsv4934570copy number variation1nstd200human GRCh38 chr6: 29,940,700-30,004,498 , GRCh37.p13 chr6: 29,908,477-29,972,275 HLA-W, POLR1HASP, 10 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4728011copy number variation2nstd197human GRCh38.p12 chr6: 29,723,465-30,109,048 , GRCh37 chr6: 29,691,242-30,076,825 HLA-A, HLA-F, 45 more genes
    nsv4436385complex substitution1nstd102humanUncertain significance GRCh38.p12 chr6: 29,942,601-30,108,066 , GRCh37 chr6: 29,910,378-30,075,843 HLA-A, HLA-J, 15 more genes
    nsv4409247copy number variation1nstd174human GRCh37 chr6: 29,910,265-29,978,544 , GRCh38.p12 chr6: 29,942,488-30,010,767 HLA-A, HLA-J, 9 more genes
    nsv4400480copy number variation1nstd174human GRCh37 chr6: 29,797,296-29,981,545 , GRCh38.p12 chr6: 29,829,519-30,013,768 MICF, HLA-A, 25 more genes
    nsv4399714copy number variation1nstd174human GRCh37 chr6: 29,871,636-29,976,968 , GRCh38.p12 chr6: 29,903,859-30,009,191 HCG4P3, POLR1HASP, 16 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv3966651copy number variation1nstd168human GRCh38 chr6: 29,801,023-30,007,774 , GRCh37.p13 chr6: 29,768,800-29,975,551 HLA-A, HLA-J, 29 more genes
    nsv3966622complex substitution1nstd168human GRCh38 chr6: 29,985,184-30,008,691 , GRCh37.p13 chr6: 29,952,961-29,976,468 HLA-J, POLR1HASP, 4 more genes
    nsv3966353insertion1nstd168human GRCh38 chr6: 29,927,805-30,020,003 , GRCh37.p13 chr6: 29,895,582-29,987,780 HLA-W, HCG4P3, 12 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
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
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