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Items: 1 to 20 of 81

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056404inversion1nstd229human GRCh38 chr7: 45,643,008-53,582,757 , GRCh37.p13 chr7: 45,682,607-53,650,450 PKD1L1, FIGNL1, 79 more genes
    nsv7054571inversion1nstd229human GRCh38 chr7: 47,367,182-50,897,080 , GRCh37.p13 chr7: 47,406,780-50,964,777 SPMIP7, ZPBP, 29 more genes
    nsv7046943inversion1nstd229human GRCh38 chr7: 45,642,996-53,582,758 , GRCh37.p13 chr7: 45,682,595-53,650,451 CDC14C, ROBO2P1, 79 more genes
    nsv7045414inversion1nstd229human GRCh38 chr7: 47,992,225-51,294,998 , GRCh37.p13 chr7: 48,031,822-51,362,695 LOC105375271, CDC14C, 22 more genes
    nsv7044479inversion1nstd229human GRCh38 chr7: 47,665,819-51,312,117 , GRCh37.p13 chr7: 47,705,417-51,379,814 GRB10, PKD1L1-AS1, 27 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6572893inversion1nstd223human GRCh38 chr7: 45,642,996-53,582,758 , GRCh37.p13 chr7: 45,682,595-53,650,451 LOC730234, LOC105375278, 79 more genes
    nsv6563914inversion1nstd223human GRCh38 chr7: 47,665,812-51,312,144 , GRCh37.p13 chr7: 47,705,410-51,379,841 DDX43P2, DDC-AS1, 27 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313509copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,778,439-50,228,656 , GRCh38.p12 chr7: 40,738,840-50,189,060 LINC01447, ABCA13, 142 more genes
    nsv6135770copy number variation1nstd213human GRCh37 chr7: 47,680,000-49,230,001 , GRCh38.p12 chr7: 47,640,402-49,190,405 HUS1, PKD1L1-AS1, 14 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5381787copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,341,583-50,171,623 , GRCh38.p12 chr7: 43,301,984-50,132,027 OGDH, LOC112267918, 110 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 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
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv3924054copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,573,756-56,174,815 , NCBI36 chr7: 40,540,281-56,142,309 , GRCh38 chr7: 40,534,157-56,107,122 VOPP1-DT, SGO1P2, 229 more genes
    nsv3919937copy number variation1nstd102humanPathogenic GRCh38 chr7: 44,571,949-53,699,760 , GRCh37 chr7: 44,611,548-53,767,453 , NCBI36 chr7: 44,578,073-53,734,947 LOC105375262, LOC105375259, 106 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3917263copy number variation1nstd102humanPathogenic GRCh38 chr7: 33,328,312-62,377,476 , GRCh37 chr7: 33,367,924-61,831,899 , NCBI36 chr7: 33,334,449-61,469,334 MIR4649, LOC107986794, 444 more genes
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