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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971035inversion1nstd209human GRCh38 chr6: 65,923,245-66,133,038 , GRCh37.p13 chr6: 66,633,138-66,842,931 NUFIP1P1, LOC105377838, 3 more genes
    nsv5845400copy number variation1nstd209human GRCh38 chr6: 66,055,233-66,110,065 , GRCh37.p13 chr6: 66,765,126-66,819,958 LOC105377839, NUFIP1P1, 1 more genes
    nsv5721403mobile element insertion1nstd211human GRCh38 chr6: 66,092,791-66,092,791 , GRCh37.p13 chr6: 66,802,684-66,802,684 NUFIP1P1
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5363115translocation1nstd200human GRCh38 chr6: 66,094,756-66,094,756 , GRCh38 chr6: 66,094,665-66,094,665 , GRCh37.p13 chr6: 66,804,558-66,804,558 , GRCh37.p13 chr6: 66,804,649-66,804,649 NUFIP1P1
    nsv5337576translocation1nstd200human GRCh37 chr6: 66,804,649-66,804,649 , GRCh37 chr6: 66,804,558-66,804,558 , GRCh38.p12 chr6: 66,094,665-66,094,665 , GRCh38.p12 chr6: 66,094,756-66,094,756 NUFIP1P1
    nsv5301061copy number variation1nstd204human GRCh38.p13 chr6: 66,079,484-66,124,373 , GRCh37.p13 chr6: 66,789,377-66,834,266 NUFIP1P1
    nsv5237827copy number variation1nstd204human GRCh38.p13 chr6: 66,094,712-66,118,691 , GRCh37.p13 chr6: 66,804,605-66,828,584 NUFIP1P1
    nsv5233268copy number variation1nstd204human GRCh38.p13 chr6: 66,079,129-66,110,965 , GRCh37.p13 chr6: 66,789,022-66,820,858 NUFIP1P1
    nsv5232393copy number variation1nstd204human GRCh38.p13 chr6: 66,079,101-66,124,300 , GRCh37.p13 chr6: 66,788,994-66,834,193 NUFIP1P1
    nsv5034374inversion1nstd200human GRCh38 chr6: 65,276,237-66,914,065 , GRCh37.p13 chr6: 65,986,130-67,623,958 LOC107986540, LOC105377841, 10 more genes
    nsv4945230copy number variation1nstd200human GRCh38 chr6: 66,079,488-66,124,370 , GRCh37.p13 chr6: 66,789,381-66,834,263 NUFIP1P1
    nsv4824444copy number variation1nstd200human GRCh37 chr6: 66,789,381-66,834,263 , GRCh38.p12 chr6: 66,079,488-66,124,370 NUFIP1P1
    nsv4708767translocation1nstd195human GRCh37 chr6: 66,803,769-66,803,769 , GRCh37 chr13: 45,523,974-45,523,974 , GRCh38.p12 chr6: 66,093,876-66,093,876 , GRCh38.p12 chr13: 44,949,839-44,949,839 NUFIP1, NUFIP1P1
    nsv4703658translocation1nstd195human GRCh37 chr6: 66,803,770-66,803,770 , GRCh37 chr13: 45,523,974-45,523,974 , GRCh38.p12 chr6: 66,093,877-66,093,877 , GRCh38.p12 chr13: 44,949,839-44,949,839 NUFIP1, NUFIP1P1
    nsv4604820copy number variation1nstd183human GRCh37 chr6: 64,732,117-73,192,183 , GRCh38.p12 chr6: 64,022,224-72,482,481 LOC105377847, LOC105377850, 64 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
    nsv4149343copy number variation1nstd166human GRCh37.p13 chr6: 66,802,443-66,810,356 , GRCh38.p12 chr6: 66,092,550-66,100,463 NUFIP1P1
    nsv4143458copy number variation1nstd166human GRCh37.p13 chr6: 65,994,849-67,582,755 , GRCh38.p12 chr6: 65,284,956-66,872,862 LOC107986540, LOC105377839, 10 more genes
    nsv3924180copy number variation1nstd102humanPathogenic NCBI36 chr6: 65,316,269-84,193,229 , GRCh38 chr6: 64,549,655-83,426,791 , GRCh37 chr6: 65,259,548-84,136,510 LOC105377875, KCNQ5-IT1, 188 more genes
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