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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950501insertion1nstd209human GRCh38 chr7: 107,591,641-107,591,641 , GRCh37.p13 chr7: 107,232,086-107,232,086 BCAP29, DUS4L-BCAP29
    nsv5918906copy number variation1nstd209human GRCh38 chr7: 107,613,649-107,613,698 , GRCh37.p13 chr7: 107,254,094-107,254,143 BCAP29, DUS4L-BCAP29
    nsv5642457insertion1nstd207human GRCh38 chr7: 107,599,227-107,599,227 , GRCh37.p13 chr7: 107,239,672-107,239,672 BCAP29, DUS4L-BCAP29
    nsv5627747insertion1nstd207human GRCh38 chr7: 107,599,231-107,599,231 , GRCh37.p13 chr7: 107,239,676-107,239,676 BCAP29, DUS4L-BCAP29
    nsv5627612insertion1nstd207human GRCh38 chr7: 107,591,641-107,591,641 , GRCh37.p13 chr7: 107,232,086-107,232,086 BCAP29, DUS4L-BCAP29
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5486581copy number variation1nstd206human GRCh38 chr7: 107,567,980-107,665,961 , GRCh37.p13 chr7: 107,208,425-107,306,406 , SLC26A4, 6 more genes
    nsv5476325copy number variation1nstd206human GRCh38 chr7: 107,582,438-107,582,499 , GRCh37.p13 chr7: 107,222,883-107,222,944 BCAP29, DUS4L-BCAP29
    nsv5370951translocation1nstd200human GRCh38 chr7: 107,617,265-107,617,265 , GRCh38 chr7: 107,641,513-107,641,513 , GRCh37.p13 chr7: 107,257,710-107,257,710 , GRCh37.p13 chr7: 107,281,958-107,281,958 , BCAP29, 2 more genes
    nsv5370949translocation1nstd200human GRCh38 chr7: 107,601,139-107,601,139 , GRCh38 chr7: 107,601,365-107,601,365 , GRCh37.p13 chr7: 107,241,810-107,241,810 , GRCh37.p13 chr7: 107,241,584-107,241,584 DUS4L-BCAP29, BCAP29
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5251783copy number variation1nstd204human GRCh38.p13 chr7: 107,617,301-107,620,000 , GRCh37.p13 chr7: 107,257,746-107,260,445 DUS4L-BCAP29, BCAP29
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4950712copy number variation1nstd200human GRCh38 chr7: 107,621,827-107,641,838 , GRCh37.p13 chr7: 107,262,272-107,282,283 , WBP1LP2, 3 more genes
    nsv4950711copy number variation1nstd200human GRCh38 chr7: 107,594,954-107,596,478 , GRCh37.p13 chr7: 107,235,399-107,236,923 DUS4L-BCAP29, BCAP29
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4819944copy number variation1nstd200human GRCh37 chr7: 107,262,272-107,282,283 , GRCh38.p12 chr7: 107,621,827-107,641,838 , BANF1P5, 3 more genes
    nsv4819943copy number variation1nstd200human GRCh37 chr7: 107,235,399-107,236,923 , GRCh38.p12 chr7: 107,594,954-107,596,478 , GRCh38.p12 chr7|NW_017852930.1: 440,609-442,133 BCAP29, DUS4L-BCAP29
    nsv4764176insertion1nstd199human GRCh37 chr7: 107,239,684-107,239,684 , GRCh38.p12 chr7: 107,599,239-107,599,239 , GRCh38.p12 chr7|NW_017852930.1: 444,894-444,894 BCAP29, DUS4L-BCAP29
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