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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959417insertion1nstd209human GRCh38 chr7: 128,386,613-128,386,613 , GRCh37.p13 chr7: 128,026,667-128,026,667 LOC107986845
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5545364insertion1nstd206human GRCh38 chr7: 128,386,613-128,386,613 , GRCh37.p13 chr7: 128,026,667-128,026,667 LOC107986845
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5104830mobile element insertion1nstd203human GRCh38 chr7: 128,386,288-128,386,304 , GRCh37.p13 chr7: 128,026,342-128,026,358 LOC107986845
    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
    nsv4968733copy number variation1nstd200human GRCh38 chr7: 128,354,799-128,479,741 , GRCh37.p13 chr7: 127,994,853-128,119,795 IMPDH1, METTL2B, 6 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4825331copy number variation1nstd200human GRCh37 chr7: 127,994,853-128,119,795 , GRCh38.p12 chr7: 128,354,799-128,479,741 IMPDH1, PRRT4, 6 more genes
    nsv4751438insertion1nstd199human GRCh37 chr7: 128,026,674-128,026,674 , GRCh38.p12 chr7: 128,386,620-128,386,620 LOC107986845
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4605769copy number variation1nstd183human GRCh37 chr7: 127,979,727-128,044,162 , GRCh38.p12 chr7: 128,339,673-128,404,108 IMPDH1, PRRT4, 3 more genes
    nsv4457011copy number variation1nstd102humanUncertain significance GRCh37 chr7: 127,999,644-128,465,294 , GRCh38.p12 chr7: 128,359,590-128,825,240 IMPDH1, GARIN1A, 20 more genes
    nsv4455826copy number variation1nstd102humanPathogenic GRCh37 chr7: 121,480,906-129,389,003 , GRCh38.p12 chr7: 121,840,852-129,749,163 ASB15, PNPT1P2, 127 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4406004copy number variation1nstd174human GRCh37 chr7: 127,978,820-128,053,377 , GRCh38.p12 chr7: 128,338,766-128,413,323 IMPDH1, RNU7-27P, 3 more genes
    nsv4322564inversion1nstd166human GRCh37.p13 chr7: 125,283,973-130,824,546 , GRCh38.p12 chr7: 125,643,919-131,139,787 , ARF5, 119 more genes
    nsv3956775copy number variation1nstd168human GRCh38 chr7: 128,373,561-128,420,713 , GRCh37.p13 chr7: 128,013,615-128,060,767 LOC107986845, IMPDH1
    nsv3923164copy number variation1nstd102humanPathogenic GRCh37 chr7: 121,658,176-128,547,780 , GRCh38 chr7: 122,018,122-128,907,727 , NCBI36 chr7: 121,445,412-128,335,016 GCC1, RNF133, 104 more genes
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