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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3899821copy number variation1nstd102humanLikely benign GRCh37 chr7: 94,399,796-94,606,785 , GRCh38.p12 chr7: 94,770,484-94,977,473 PPP1R9A, ARF1P1, 2 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 PPP1R9A, 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 PPP1R9A, LOC107986817, 2014 more genes
    nsv3914094copy number variation1nstd102humanPathogenic GRCh38 chr7: 84,002,634-95,228,883 , GRCh37 chr7: 83,631,950-94,858,195 , NCBI36 chr7: 83,469,886-94,696,131 PPP1R9A, LINC03017, 121 more genes
    nsv3892887copy number variation1nstd102humanPathogenic GRCh37 chr7: 92,445,452-99,686,985 , GRCh38.p12 chr7: 92,816,138-100,089,362 PPP1R9A, LOC105375402, 153 more genes
    nsv6636271copy number variation1nstd102humanPathogenic GRCh37 chr7: 92,721,627-98,311,537 , GRCh38.p12 chr7: 93,092,314-98,682,225 PPP1R9A, MARK2P10, 97 more genes
    nsv3911538copy number variation1nstd102humanPathogenic NCBI36 chr7: 92,226,394-97,035,894 , GRCh38 chr7: 92,759,144-97,568,646 , GRCh37 chr7: 92,388,458-97,197,958 PPP1R9A, LOC105375410, 75 more genes
    nsv3901032copy number variation1nstd102humanPathogenic GRCh37 chr7: 93,700,162-96,950,914 , GRCh38.p12 chr7: 94,070,850-97,321,602 PPP1R9A, LOC105375404, 52 more genes
    nsv3908984copy number variation1nstd102humanPathogenic GRCh37 chr7: 93,285,237-96,280,817 , GRCh38.p12 chr7: 93,655,925-96,651,505 PPP1R9A, LOC105375402, 51 more genes
    nsv3922980copy number variation1nstd102humanPathogenic GRCh37 chr7: 94,756,382-97,502,799 , GRCh38 chr7: 95,127,070-97,873,487 , NCBI36 chr7: 94,594,318-97,340,735 PPP1R9A, RNU6-532P, 41 more genes
    nsv4685981copy number variation1nstd102humanPathogenic GRCh37 chr7: 93,516,132-95,668,733 , GRCh38.p12 chr7: 93,886,820-96,039,421 PPP1R9A, LOC105375404, 36 more genes
    nsv3916221copy number variation1nstd102humanPathogenic NCBI36 chr7: 92,754,488-94,797,369 , GRCh37.p13 chr7: 92,916,552-94,959,433 , GRCh38.p12 chr7: 93,287,240-95,330,121 PPP1R9A, BET1-AS1, 33 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 PPP1R9A, RNU6-565P, 2684 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 PPP1R9A, RPL23AP51, 2684 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 PPP1R9A, MNX1-AS2, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 PPP1R9A, TRGV3, 2682 more genes
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 PPP1R9A, ARPC1A, 265 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 PPP1R9A, AOC1, 2682 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 PPP1R9A, ACHE, 1532 more genes
    nsv3909475copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 94,129,826-94,844,077 , GRCh38.p12 chr7: 94,500,514-95,214,765 PPP1R9A, SGCE, 12 more genes
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