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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 NOBOX, FAM131B, 466 more genes
    nsv7057176inversion1nstd229human GRCh38 chr7: 142,200,564-149,795,026 , GRCh37.p13 chr7: 141,988,816-149,492,114 RN7SL72P, RPL32P17, 258 more genes
    nsv7051735inversion1nstd229human GRCh38 chr7: 142,037,473-144,135,486 , GRCh37.p13 chr7: 141,988,816-143,832,579 LOC105375546, TRBV21-1, 162 more genes
    nsv7050513inversion1nstd229human GRCh38 chr7: 144,064,087-144,131,336 , GRCh37.p13 chr7: 143,761,180-143,828,429 OR2A15P, OR2A14, 5 more genes
    nsv7049746inversion1nstd229human GRCh38 chr7: 143,132,164-144,147,382 , GRCh37.p13 chr7: 142,829,257-143,844,475 RPL26P24, EPHA1, 55 more genes
    nsv6829632copy number variation1nstd229human GRCh38 chr7: 144,080,418-144,116,927 , GRCh37.p13 chr7: 143,777,511-143,814,020 OR2A15P, OR2A12, 2 more genes
    nsv6825505copy number variation1nstd229human GRCh38 chr7: 144,091,601-144,100,700 , GRCh37.p13 chr7: 143,788,694-143,797,793 OR2A12
    nsv6823453copy number variation1nstd229human GRCh38 chr7: 144,091,627-144,099,009 , GRCh37.p13 chr7: 143,788,720-143,796,102 OR2A12
    nsv6818908copy number variation1nstd229human GRCh38 chr7: 144,091,176-144,093,294 , GRCh37.p13 chr7: 143,788,269-143,790,387 OR2A12
    nsv6636458copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643 TRBD2, TRBV5-2, 403 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
    nsv6631783copy number variation1nstd224human GRCh37 chr7: 143,426,263-143,874,190 , GRCh38.p12 chr7: 143,729,170-144,177,097 , GRCh38.p12 chr7|NW_018654714.1: 273,489-589,656 TCAF1, OR2F1, 25 more genes
    nsv6631576copy number variation1nstd224human GRCh37 chr7: 143,429,038-143,870,422 , GRCh38.p12 chr7: 143,731,945-144,173,329 , GRCh38.p12 chr7|NW_018654714.1: 276,264-589,656 TCAF1, OR2A15P, 23 more genes
    nsv6424450copy number variation1nstd223human GRCh38 chr7: 144,091,627-144,099,007 , GRCh37.p13 chr7: 143,788,720-143,796,100 OR2A12
    nsv6315434copy number variation1nstd102humanUncertain significance GRCh37 chr7: 143,425,718-144,075,390 , GRCh38.p12 chr7|NW_018654715.1: 1-409,704 , GRCh38.p12 chr7: 143,728,625-144,378,297 ARHGEF5, ARHGEF34P, 41 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6291163copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,851,002-159,119,707 , GRCh38.p12 chr7: 134,166,250-159,327,017 TRB, ZC3HAV1L, 579 more genes
    nsv6290262copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,848,099-145,814,115 , GRCh38.p12 chr7: 134,163,347-146,117,023 TRBJ2-7, PRSS2, 341 more genes
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