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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
    nsv7097867copy number variation1nstd102humanUncertain significance GRCh37 chr7: 142,456,998-142,457,385 , GRCh38.p12 chr7|NT_187562.1: 751,744-752,131 TRB, PRSS1
    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
    nsv7051466inversion1nstd229human GRCh38 chr7: 142,234,514-142,870,862 , GRCh37.p13 chr7: 141,988,816-142,568,615 , GRCh37.p13 chr7|NW_003571040.1: 512,000-1,033,264 TRBV19, PRSS3P1, 95 more genes
    nsv7046649inversion1nstd229human GRCh38 chr7: 142,280,484-143,114,495 , GRCh37.p13 chr7: 141,988,816-142,811,588 , GRCh37.p13 chr7|NW_003571040.1: 422,455-1,127,132 TRBJ2-1, TRBV7-6, 101 more genes
    nsv7042191inversion1nstd229human GRCh38 chr7: 142,234,497-142,870,862 , GRCh37.p13 chr7: 141,988,816-142,568,615 , GRCh37.p13 chr7|NW_003571040.1: 512,000-1,033,264 TRBJ1-6, TRBV20-1, 95 more genes
    nsv6835202copy number variation1nstd229human GRCh38 chr7: 142,736,990-142,738,773 , GRCh37.p13 chr7: 142,444,836-142,446,619 TRB, PRSS1, 1 more genes
    nsv6832172copy number variation1nstd229human GRCh38 chr7: 142,451,409-142,796,368 , GRCh37.p13 chr7|NW_003571040.1: 705,943-999,412 TRBV5-4, TRBJ1-2, 62 more genes
    nsv6830202copy number variation1nstd229human GRCh38 chr7: 142,747,801-142,818,200 , GRCh37.p13 chr7: 142,455,652-142,494,030 TRB, TRBV30, 23 more genes
    nsv6829591copy number variation1nstd229human GRCh38 chr7: 142,451,444-142,796,372 , GRCh37.p13 chr7|NW_003571040.1: 705,943-999,416 TRBV7-5, PRSS2, 62 more genes
    nsv6827995copy number variation1nstd229human GRCh38 chr7: 142,408,128-142,787,017 , GRCh37.p13 chr7|NW_003571040.1: 705,943-990,061 TRBV6-6, TRBJ1-6, 57 more genes
    nsv6827355copy number variation1nstd229human GRCh38 chr7: 142,578,301-142,753,300 , GRCh37.p13 chr7: 142,326,199-142,461,151 TRBV18, TRBV29-1, 21 more genes
    nsv6826880copy number variation1nstd229human GRCh38 chr7: 142,715,856-142,787,068 , GRCh37.p13 chr7: 142,423,683-142,494,030 TRBJ1-4, PRSS1, 14 more genes
    nsv6818658copy number variation1nstd229human GRCh38 chr7: 142,301,428-142,787,019 , GRCh37.p13 chr7|NW_003571040.1: 512,000-990,063 , GRCh37.p13 chr7: 142,001,251-142,494,030 TRBV11-2, TRBV12-2, 75 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
    nsv6631841copy number variation1nstd224human GRCh37 chr7: 142,459,680-142,481,317 , GRCh38.p12 chr7|NT_187562.1: 754,426-776,063 TRB, PRSS3P2, 2 more genes
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