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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6309637copy number variation1nstd102humanUncertain significance GRCh37 chr15: 82,443,786-82,444,784 , GRCh38.p12 chr15: 82,151,445-82,152,443 EFL1
    nsv7094309copy number variation1nstd102humanUncertain significance GRCh37 chr15: 82,511,973-82,512,590 , GRCh38.p12 chr15: 82,219,632-82,220,249 EFL1
    nsv3918341copy number variation1nstd102humanLikely benign NCBI36 chr15: 80,207,288-80,338,274 , GRCh37 chr15: 82,420,233-82,551,219 , GRCh38 chr15: 82,127,892-82,258,878 EFL1, RNU1-77P
    nsv6309638copy number variation1nstd102humanUncertain significance GRCh37 chr15: 82,511,973-82,554,119 , GRCh38.p12 chr15: 82,219,632-82,261,778 EFL1, SAXO2
    nsv7094736copy number variation1nstd102humanUncertain significance GRCh37 chr15: 82,545,012-82,554,119 , GRCh38.p12 chr15: 82,252,671-82,261,778 EFL1, SAXO2
    nsv3898713copy number variation1nstd102humanBenign GRCh37 chr15: 82,451,027-82,595,565 , GRCh38.p12 chr15: 82,158,686-82,303,227 EFL1, ADAMTS7P1, 2 more genes
    nsv7094637copy number variation1nstd102humanUncertain significance GRCh37 chr15: 82,456,174-82,554,119 , GRCh38.p12 chr15: 82,163,833-82,261,778 EFL1, SAXO2, 1 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 CRB1, STX6, 1608 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 EFL1, H3P40, 1616 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 EFL1, RNU6-18P, 1442 more genes
    nsv4456639copy number variation1nstd102humanPathogenic GRCh37 chr15: 80,728,654-84,107,646 , GRCh38.p12 chr15: 80,436,313-83,438,894 EFL1, LOC100288241, 64 more genes
    nsv3905472copy number variation1nstd102humanPathogenic GRCh37 chr15: 80,703,867-83,955,596 , GRCh38.p12 chr15: 80,411,525-83,286,844 EFL1, LINC01583, 62 more genes
    nsv3906070copy number variation1nstd102humanPathogenic NCBI36 chr1: 152,814,789-153,529,316 , GRCh37 chr1: 154,548,165-155,262,692 , GRCh38 chr1: 154,575,689-155,292,901 PBXIP1, ZBTB7B, 37 more genes
    nsv7148244copy number variation1nstd102humanPathogenic GRCh38 chr15: 82,130,136-82,727,529 , GRCh37.p13 chr15: 82,422,477-83,396,281 EFL1, CPEB1-AS1, 22 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 MARK1, LINC02766, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 SNAP47, STK40, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 RNU1-153P, MIR3917, 4887 more genes
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 LOC101060227, LINC01720, 1608 more genes
    nsv3900281copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337 EFL1, MYZAP, 1750 more genes
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 EFL1, MIR4513, 1754 more genes
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