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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
    nsv7137336copy number variation1nstd232human GRCh37.p13 chr7: 148,480,980-148,481,059 , GRCh38.p12 chr7: 148,783,888-148,783,967 CUL1
    nsv7097871copy number variation1nstd102humanUncertain significance GRCh37 chr7: 145,813,969-148,544,390 , GRCh38.p12 chr7: 146,116,877-148,847,298 LOC105375554, MIR548F4, 20 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
    nsv7097613copy number variation1nstd102humanUncertain significance GRCh37 chr7: 147,600,637-148,544,390 , GRCh38.p12 chr7: 147,903,545-148,847,298 LOC643438, RN7SL456P, 11 more genes
    nsv7097350copy number variation1nstd102humanPathogenic GRCh37 chr7: 146,471,343-148,544,390 , GRCh38.p12 chr7: 146,774,251-148,847,298 CNTNAP2, RNU7-20P, 19 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
    nsv7053112inversion1nstd229human GRCh38 chr7: 148,687,579-148,700,720 , GRCh37.p13 chr7: 148,384,671-148,397,812 CUL1
    nsv7052478inversion1nstd229human GRCh38 chr7: 148,598,936-149,120,264 , GRCh37.p13 chr7: 148,296,028-148,817,356 RNY1, CUL1, 16 more genes
    nsv7046837inversion1nstd229human GRCh38 chr7: 146,996,779-152,901,438 , GRCh37.p13 chr7: 146,693,871-152,598,523 RARRES2, RN7SL76P, 153 more genes
    nsv7040762inversion1nstd229human GRCh38 chr7: 148,598,948-149,120,315 , GRCh37.p13 chr7: 148,296,040-148,817,407 RNU6-650P, COX6B1P1, 16 more genes
    nsv6833161copy number variation1nstd229human GRCh38 chr7: 148,755,872-148,756,348 , GRCh37.p13 chr7: 148,452,964-148,453,440 CUL1
    nsv6833013copy number variation1nstd229human GRCh38 chr7: 148,795,962-148,804,655 , GRCh37.p13 chr7: 148,493,054-148,501,747 CUL1
    nsv6831366copy number variation1nstd229human GRCh38 chr7: 148,655,201-148,717,400 , GRCh37.p13 chr7: 148,352,293-148,414,492 CUL1
    nsv6828845copy number variation1nstd229human GRCh38 chr7: 148,749,101-148,758,900 , GRCh37.p13 chr7: 148,446,193-148,455,992 CUL1
    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
    nsv6558271inversion1nstd223human GRCh38 chr7: 148,751,869-148,752,622 , GRCh37.p13 chr7: 148,448,961-148,449,714 CUL1
    nsv6558115inversion1nstd223human GRCh38 chr7: 146,996,771-152,901,398 , GRCh37.p13 chr7: 146,693,863-152,598,483 ZNF398, PRKAG2-AS1, 153 more genes
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