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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
    nsv7049746inversion1nstd229human GRCh38 chr7: 143,132,164-144,147,382 , GRCh37.p13 chr7: 142,829,257-143,844,475 RPL26P24, EPHA1, 55 more genes
    nsv6828546copy number variation1nstd229human GRCh38 chr7: 143,882,211-143,889,812 , GRCh37.p13 chr7: 143,579,304-143,586,905 TCAF1, LOC105375549
    nsv6823135copy number variation1nstd229human GRCh38 chr7: 143,893,211-143,947,450 , GRCh37.p13 chr7: 143,590,304-143,644,543 OR2F2, LOC105375549, 2 more genes
    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
    nsv6431879copy number variation1nstd223human GRCh38 chr7: 143,840,801-143,851,600 , GRCh37.p13 chr7: 143,537,894-143,548,693 TCAF1, LOC112267988
    nsv6431273copy number variation1nstd223human GRCh38 chr7: 143,829,301-143,861,000 , GRCh37.p13 chr7: 143,526,394-143,558,093 TCAF1, LOC154761, 1 more genes
    nsv6427602copy number variation1nstd223human GRCh38 chr7: 143,893,211-143,947,445 , GRCh37.p13 chr7: 143,590,304-143,644,538 OR2F1, TCAF1, 2 more genes
    nsv6423895copy number variation1nstd223human GRCh38 chr7: 143,844,901-143,863,400 , GRCh37.p13 chr7: 143,541,994-143,560,493 LOC112267988, TCAF1
    nsv6418893copy number variation1nstd223human GRCh38 chr7: 143,836,201-143,890,100 , GRCh37.p13 chr7: 143,533,294-143,587,193 LOC112267988, LOC105375549, 2 more genes
    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
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