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Items: 1 to 20 of 163

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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
    nsv7041666inversion1nstd229human GRCh38 chr7: 143,406,037-143,406,119 , GRCh37.p13 chr7: 143,103,130-143,103,212 EPHA1, EPHA1-AS1
    nsv6828881copy number variation1nstd229human GRCh38 chr7: 143,198,701-143,410,900 , GRCh37.p13 chr7: 142,895,794-143,107,993 EPHA1, FAM131B, 15 more genes
    nsv6825726copy number variation1nstd229human GRCh38 chr7: 143,291,701-143,439,700 , GRCh37.p13 chr7: 142,988,794-143,136,793 RN7SL481P, ZYX, 10 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
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313607copy number variation1nstd102humanUncertain significance GRCh37 chr7: 142,691,458-143,193,361 , GRCh38.p12 chr7: 142,994,373-143,496,268 FAM131B, TAS2R62P, 27 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
    nsv6136967copy number variation1nstd213human GRCh37 chr7: 142,970,000-143,090,001 , GRCh38.p12 chr7: 143,272,907-143,392,908 FAM131B-AS2, MIR6892, 11 more genes
    nsv6135972copy number variation1nstd213human GRCh37 chr7: 142,120,000-143,090,001 , GRCh38.p12 chr7: 142,618,685-143,392,908 , GRCh38.p12 chr7|NT_187562.1: 622,348-1,111,570 , CASP2, 70 more genes
    nsv6135900copy number variation1nstd213human GRCh37 chr7: 142,330,000-143,440,001 , GRCh38.p12 chr7: 142,622,486-143,742,908 , EPHA1, 82 more genes
    nsv6135899copy number variation1nstd213human GRCh37 chr7: 142,330,000-143,270,001 , GRCh38.p12 chr7: 142,622,486-143,572,908 , GRCh38.p12 chr7|NT_187562.1: 626,148-1,111,570 , CLCN1, 80 more genes
    nsv6135568copy number variation1nstd213human GRCh37 chr7: 142,100,000-143,170,001 , GRCh38.p12 chr7: 142,618,685-143,472,908 , CASP2, 71 more genes
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