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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6312536copy number variation1nstd102humanUncertain significance GRCh37 chr7: 17,373,516-17,382,688 , GRCh38.p12 chr7: 17,333,892-17,343,064 AHR
    nsv4681712copy number variation1nstd102humanUncertain significance GRCh37 chr7: 17,338,889-17,382,688 , GRCh38.p12 chr7: 17,299,265-17,343,064 AHR
    nsv7097616copy number variation1nstd102humanUncertain significance GRCh37 chr7: 17,349,540-17,382,688 , GRCh38.p12 chr7: 17,309,916-17,343,064 AHR
    nsv3905003copy number variation1nstd102humanBenign GRCh37 chr7: 17,326,058-17,384,210 , GRCh38.p12 chr7: 17,286,434-17,344,586 AHR, LOC101927609
    nsv3917904copy number variation1nstd102humanLikely benign NCBI36 chr7: 16,931,199-17,340,221 , GRCh37 chr7: 16,964,674-17,373,696 , GRCh38 chr7: 16,925,050-17,334,072 AHR, LOC105375170, 3 more genes
    nsv3905995copy number variation1nstd102humanBenign GRCh37 chr7: 17,383,107-17,629,311 , GRCh38.p12 chr7: 17,343,483-17,589,687 AHR, LINC02889, 3 more genes
    nsv3905671copy number variation1nstd102humanBenign GRCh37 chr7: 17,384,210-17,629,654 , GRCh38.p12 chr7: 17,344,586-17,590,030 AHR, LOC105375172, 3 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 AHR, RNU6-438P, 2682 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 AHR, LOC107986817, 2014 more genes
    nsv3915219copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,649,696-25,800,180 , GRCh38 chr7: 10,610,069-25,760,560 , NCBI36 chr7: 10,616,221-25,766,705 AHR, SNORD93, 176 more genes
    nsv6313854copy number variation1nstd102humanPathogenic GRCh37 chr7: 9,358,316-20,982,082 , GRCh38.p12 chr7: 9,318,686-20,942,463 AHR, LOC107986766, 115 more genes
    nsv3913922copy number variation1nstd102humanPathogenic GRCh38 chr7: 9,975,653-19,356,878 , NCBI36 chr7: 9,981,805-19,363,026 , GRCh37 chr7: 10,015,280-19,396,501 AHR, NPM1P13, 86 more genes
    nsv3911741copy number variation1nstd102humanPathogenic GRCh37 chr7: 15,573,437-24,891,051 , GRCh38 chr7: 15,533,812-24,851,432 , NCBI36 chr7: 15,539,962-24,857,576 AHR, LINC01162, 124 more genes
    nsv3912345copy number variation1nstd102humanPathogenic NCBI36 chr7: 8,962,614-17,387,487 , GRCh37.p13 chr7: 8,996,089-17,420,962 , GRCh38.p12 chr7: 8,956,459-17,381,338 AHR, RAD17P1, 78 more genes
    nsv4674987copy number variation1nstd102humanPathogenic GRCh37 chr7: 13,886,653-20,267,202 , GRCh38.p12 chr7: 13,847,028-20,227,579 AHR, BZW2, 64 more genes
    nsv4768371copy number variation1nstd102humanPathogenic GRCh37 chr7: 14,470,668-20,385,165 , GRCh38.p12 chr7: 14,431,043-20,345,542 AHR, HDAC9, 60 more genes
    nsv3910744copy number variation1nstd102humanPathogenic GRCh38 chr7: 15,133,711-19,642,829 , GRCh37 chr7: 15,173,336-19,682,452 , NCBI36 chr7: 15,139,861-19,648,977 AHR, LOC105375171, 44 more genes
    nsv3922488copy number variation1nstd102humanPathogenic GRCh37 chr7: 16,161,141-20,647,522 , GRCh38 chr7: 16,121,516-20,607,899 , NCBI36 chr7: 16,127,666-20,614,047 AHR, HDAC9, 53 more genes
    nsv3912914copy number variation1nstd102humanPathogenic GRCh37 chr7: 14,005,822-18,360,977 , GRCh38 chr7: 13,966,197-18,321,354 , NCBI36 chr7: 13,972,347-18,327,502 AHR, RPL36AP26, 43 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 AHR, RNU6-565P, 2684 more genes
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