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Items: 1 to 20 of 126

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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
    nsv7097607copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 138,391,369-141,759,786 , GRCh38.p12 chr7: 138,706,624-142,059,986 LOC105375535, AGK-DT, 82 more genes
    nsv6818506copy number variation1nstd229human GRCh38 chr7: 138,935,833-139,457,377 , GRCh37.p13 chr7: 138,620,579-139,142,123 RNU6-206P, MIR10399, 17 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
    nsv6567612inversion1nstd223human GRCh38 chr7: 139,184,793-139,350,399 , GRCh37.p13 chr7: 138,869,539-139,035,145 LUC7L2, IFT56, 7 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6312322copy number variation1nstd102humanUncertain significance GRCh37 chr7: 137,761,265-141,759,786 , GRCh38.p12 chr7: 138,076,519-142,059,986 RPS17P12, RNU6-85P, 96 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
    nsv6136963copy number variation1nstd213human GRCh37 chr7: 138,680,000-139,030,001 , GRCh38.p12 chr7: 138,995,254-139,345,255 LUC7L2, ZC3HAV1L, 13 more genes
    nsv6135563copy number variation1nstd213human GRCh37 chr7: 137,560,000-142,040,001 , GRCh38.p12 chr7: 137,875,254-142,288,986 NDUFB2, SSBP1, 105 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
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4958648copy number variation1nstd200human GRCh38 chr7: 139,345,255-139,345,478 , GRCh37.p13 chr7: 139,030,001-139,030,224 FMC1, LUC7L2, 1 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4676044copy number variation1nstd102humanPathogenic GRCh37 chr7: 135,677,938-139,810,886 , GRCh38.p12 chr7: 135,993,190-140,111,086 SVOPL, RPS17P12, 62 more genes
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