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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924916copy number variation1nstd209human GRCh38 chr7: 98,880,601-98,880,796 , GRCh37.p13 chr7|NW_003571041.1: 249,783-249,978 , GRCh37.p13 chr7: 98,478,224-98,478,419 TRRAP, SCARNA28, 1 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
    nsv5492189copy number variation1nstd206human GRCh38 chr7: 98,880,601-98,880,800 , GRCh37.p13 chr7|NW_003571041.1: 249,783-249,982 , GRCh37.p13 chr7: 98,478,224-98,478,423 MIR3609, TRRAP, 1 more genes
    nsv5477176copy number variation1nstd206human GRCh38 chr7: 98,880,235-98,880,290 , GRCh37.p13 chr7|NW_003571041.1: 249,417-249,472 , GRCh37.p13 chr7: 98,477,858-98,477,913 SCARNA28, TRRAP, 1 more genes
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 more genes
    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
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4729043copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,277,871-98,483,457 , GRCh38.p12 chr7: 98,648,559-98,885,834 MIR3609, LOC105375418, 5 more genes
    nsv4610409copy number variation1nstd183human GRCh37 chr7: 98,366,565-98,560,243 , GRCh38.p12 chr7: 98,737,253-98,962,620 TMEM130, MIR3609, 3 more genes
    nsv4524999copy number variation1nstd166human GRCh37.p13 chr7: 98,478,224-98,478,423 , GRCh38.p12 chr7: 98,880,601-98,880,800 SCARNA28, MIR3609, 1 more genes
    nsv4456313copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,373,794-98,676,268 , GRCh38.p12 chr7: 98,744,482-99,078,645 TMEM130, RNU6-393P, 6 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
    nsv4159940copy number variation1nstd166human GRCh37.p13 chr7: 98,370,136-98,667,372 , GRCh38.p12 chr7: 98,740,824-99,069,749 TRRAP, SMURF1, 6 more genes
    nsv4157654copy number variation1nstd166human GRCh37.p13 chr7: 98,477,858-98,477,913 , GRCh38.p12 chr7: 98,880,235-98,880,290 MIR3609, TRRAP, 1 more genes
    nsv3922815copy number variation1nstd102humanPathogenic NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453 SEPTIN7P6, MIR93, 1175 more genes
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