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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5910215copy number variation1nstd209human GRCh38 chr7: 99,454,134-99,456,428 , GRCh37.p13 chr7: 99,051,757-99,054,051 ATP5MF, CPSF4, 1 more genes
    nsv5632499insertion1nstd207human GRCh38 chr7: 99,440,674-99,440,674 , GRCh37.p13 chr7: 99,038,297-99,038,297 CPSF4, LOC100131859, 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
    nsv5475371copy number variation1nstd206human GRCh38 chr7: 99,444,261-99,444,503 , GRCh37.p13 chr7: 99,041,884-99,042,126 ATP5MF-PTCD1, CPSF4
    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
    nsv5258181copy number variation1nstd204human GRCh38.p13 chr7: 99,420,101-99,576,000 , GRCh37.p13 chr7: 99,017,724-99,173,623 TMEM225B, ZNF394, 13 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
    nsv4455239copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,758,955-99,368,262 , GRCh38.p12 chr7: 99,161,332-99,770,639 TMEM225B, CYP3A7-CYP3A51P, 28 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
    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
    nsv3922535copy number variation1nstd102humanLikely benign NCBI36 chr7: 98,631,395-99,783,622 , GRCh37 chr7: 98,793,459-99,945,686 , GRCh38 chr7: 99,195,836-100,348,063 LAMTOR4, MIR12119, 66 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
    nsv3916333copy number variation1nstd102humanPathogenic GRCh37 chr7: 97,917,786-100,903,085 , GRCh38 chr7: 98,288,474-101,259,804 , NCBI36 chr7: 97,755,722-100,689,805 ZCWPW1, LOC101927610, 141 more genes
    nsv3915692copy number variation1nstd102humanPathogenic GRCh38 chr7: 99,195,836-102,258,175 , NCBI36 chr7: 98,631,395-101,688,175 , GRCh37 chr7: 98,793,459-101,718,950 MUC17, LOC107986829, 135 more genes
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