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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5915154copy number variation1nstd209human GRCh37.p13 chr7: 84,361-315,646 , GRCh38 chr7: 84,361-275,680 FAM20C, LINC03014, 4 more genes
    nsv5846423copy number variation2nstd209human GRCh38 chr7: 171,608-193,851 , GRCh37.p13 chr7: 171,608-193,851 LOC105375115, FAM20C, 1 more genes
    nsv5846419copy number variation2nstd209human GRCh38 chr7: 169,424-175,243 , GRCh37.p13 chr7: 169,424-175,243 LOC105375115, LOC105375116
    nsv5626732insertion1nstd207human GRCh38 chr7: 173,031-173,031 , GRCh37.p13 chr7: 173,031-173,031 LOC105375115
    nsv5579444copy number variation1nstd207human GRCh38 chr7: 173,007-173,066 , GRCh37.p13 chr7: 173,007-173,066 LOC105375115
    nsv5467704copy number variation1nstd206human GRCh38 chr7: 106,098-179,488 , GRCh37.p13 chr7: 106,098-179,488 LOC105375115, LINC03015, 3 more genes
    nsv5454390copy number variation1nstd206human GRCh38 chr7: 136,433-405,503 , GRCh37.p13 chr7: 136,433-445,469 FAM20C, LOC442497, 7 more genes
    nsv4966117copy number variation1nstd200human GRCh38 chr7: 174,705-189,947 , GRCh37.p13 chr7: 174,705-189,947 LOC105375115, LOC105375116
    nsv4953172copy number variation1nstd200human GRCh38 chr7: 85,177-322,256 , GRCh37.p13 chr7: 85,177-362,222 LINC03015, LOC105375116, 6 more genes
    nsv4824944copy number variation1nstd200human GRCh37 chr7: 170,286-425,176 , GRCh38.p12 chr7: 170,286-385,210 FAM20C, LOC105375116, 5 more genes
    nsv4824943copy number variation1nstd200human GRCh37 chr7: 133,773-198,796 , GRCh38.p12 chr7: 133,773-198,796 , GRCh38.p12 chr7|NT_187653.1: 126,094-190,923 , GRCh38.p12 chr7|NT_187558.1: 89,695-158,006 LOC105375115, LINC03014, 3 more genes
    nsv4818193copy number variation1nstd200human GRCh37 chr7: 174,705-189,947 , GRCh38.p12 chr7|NT_187653.1: 167,026-182,268 , GRCh38.p12 chr7|NT_187558.1: 134,109-149,351 , GRCh38.p12 chr7: 174,705-189,947 LOC105375115, LOC105375116
    nsv4729558copy number variation1nstd102humanLikely benign GRCh37 chr7: 154,720-230,772 , GRCh38.p12 chr7: 154,720-230,772 , GRCh38.p12 chr7|NT_187558.1: 110,525-157,952 , GRCh38.p12 chr7|NT_187653.1: 147,041-190,869 FAM20C, LINC03014, 2 more genes
    nsv4679986copy number variation1nstd189human GRCh37.p13 chr7: 1-551,584 , GRCh38.p12 chr7: 10,001-511,947 , PDGFA, 16 more genes
    nsv4679256copy number variation1nstd189human GRCh37.p13 chr7: 1-210,544 , GRCh38.p12 chr7: 10,001-210,544 , GRCh38.p12 chr7|NT_187558.1: 1-157,952 , GRCh38.p12 chr7|NT_187653.1: 1-190,869 , FAM20C, 9 more genes
    nsv4675871copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-1,750,797 , GRCh38.p12 chr7: 44,935-1,711,161 C7orf50, LOC105375123, 47 more genes
    nsv4675301copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-1,648,288 , GRCh38.p12 chr7: 43,360-1,608,652 LOC112267991, MICALL2, 42 more genes
    nsv4602451copy number variation1nstd183human GRCh37 chr7: 175,048-231,145 , GRCh38.p12 chr7: 175,048-231,145 LOC105375115, FAM20C, 1 more genes
    nsv4601973copy number variation2nstd183human GRCh37 chr7: 145,185-197,471 , GRCh38.p12 chr7: 145,185-197,471 , GRCh38.p12 chr7|NT_187558.1: 100,984-156,875 , GRCh38.p12 chr7|NT_187653.1: 137,506-189,792 LOC105375115, FAM20C, 3 more genes
    nsv4523970copy number variation1nstd166human GRCh37.p13 chr7: 170,321-425,134 , GRCh38.p12 chr7: 170,321-385,168 FAM20C, LOC442497, 5 more genes
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