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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
    nsv7057805inversion1nstd229human GRCh38 chr7: 144,229,946-144,388,138 , GRCh37.p13 chr7: 143,927,039-144,085,231 OR2A42, OR2A9P, 8 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
    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
    nsv6424302copy number variation1nstd223human GRCh38 chr7: 144,379,461-144,386,454 , GRCh37.p13 chr7: 144,076,554-144,083,547 ARHGEF5
    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
    nsv6136970copy number variation1nstd213human GRCh37 chr7: 144,040,000-146,410,001 , GRCh38.p12 chr7: 144,342,907-146,712,909 CNTNAP2, LOC402715, 14 more genes
    nsv6135975copy number variation1nstd213human GRCh37 chr7: 144,030,000-144,450,001 , GRCh38.p12 chr7: 144,332,907-144,752,908 ARHGEF5, TPK1, 5 more genes
    nsv6135974copy number variation1nstd213human GRCh37 chr7: 144,020,000-144,670,001 , GRCh38.p12 chr7: 144,322,907-144,972,908 , GRCh38.p12 chr7|NW_018654715.1: 277,521-680,662 ARHGEF5, EEF1A1P10, 10 more genes
    nsv6135572copy number variation1nstd213human GRCh37 chr7: 144,020,000-144,850,001 , GRCh38.p12 chr7: 144,322,907-145,152,908 ARHGEF5, EI24P4, 10 more genes
    nsv6116903copy number variation1nstd186human GRCh37 chr7: 143,889,897-144,073,897 , GRCh38.p12 chr7: 144,192,804-144,376,804 , ARHGEF35-AS1, 10 more genes
    nsv6064586insertion1nstd212human GRCh38 chr7: 144,379,377-144,379,377 , GRCh37.p13 chr7: 144,076,470-144,076,470 ARHGEF5
    nsv6016252copy number variation1nstd212human GRCh38 chr7: 144,180,403-144,377,283 , GRCh37.p13 chr7: 143,877,496-144,074,376 , OR2A1, 11 more genes
    nsv5669982inversion1nstd207human GRCh37.p13 chr7: 143,979,413-144,075,887 , GRCh38 chr7: 144,282,320-144,378,794 ARHGEF5, OR2A1, 4 more genes
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