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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137141copy number variation1nstd102humanPathogenic GRCh38 chr2: 110,091,573-110,212,811 , GRCh37.p13 chr2: 110,849,150-110,970,388 MALL, ACTR1AP1, 2 more genes
    nsv7052468inversion1nstd229human GRCh38 chr2: 109,726,921-110,637,321 , GRCh37.p13 chr2: 110,484,498-111,394,898 LOC105373553, NPHP1, 39 more genes
    nsv7038094inversion1nstd229human GRCh38 chr2: 106,480,616-110,213,336 , GRCh37.p13 chr2: 107,097,072-110,970,913 WASF1P1, LOC105373985, 72 more genes
    nsv6697969copy number variation1nstd229human GRCh38 chr2: 110,095,101-110,258,100 , GRCh37.p13 chr2: 110,852,678-111,015,677 MALL, LOC100507334, 3 more genes
    nsv6694714copy number variation1nstd229human GRCh38 chr2: 110,095,201-110,228,200 , GRCh37.p13 chr2: 110,852,778-110,985,777 NPHP1, MTLN, 2 more genes
    nsv6692400copy number variation1nstd229human GRCh38 chr2: 110,098,005-110,101,352 , GRCh37.p13 chr2: 110,855,582-110,858,929 MALL
    nsv6687518copy number variation1nstd229human GRCh38 chr2: 110,105,001-110,228,600 , GRCh37.p13 chr2: 110,862,578-110,986,177 MTLN, NPHP1, 2 more genes
    nsv6686545copy number variation1nstd229human GRCh38 chr2: 103,585,907-110,943,040 , GRCh37.p13 chr2: 104,202,365-111,700,617 PPP1R2P5, CAPZBP1, 142 more genes
    nsv6682274copy number variation1nstd229human GRCh38 chr2: 110,080,401-110,228,200 , GRCh37.p13 chr2: 110,837,978-110,985,777 MTLN, MALL, 3 more genes
    nsv6679287copy number variation1nstd229human GRCh38 chr2: 110,077,301-110,311,100 , GRCh37.p13 chr2: 110,834,878-111,068,677 LOC100507334, ACTR1AP1, 5 more genes
    nsv6635291copy number variation1nstd227human GRCh38.p12 chr2: 110,095,298-110,222,769 , GRCh37 chr2: 110,852,875-110,980,346 NPHP1, MALL, 2 more genes
    nsv6634903copy number variation1nstd227human GRCh37 chr2: 110,477,792-110,980,346 , GRCh38.p12 chr2: 109,720,215-110,222,769 NPHP1, MALL, 23 more genes
    nsv6634363copy number variation1nstd102humanUncertain significance GRCh37 chr2: 110,498,141-111,365,996 , GRCh38.p12 chr2: 109,740,564-110,608,419 NPHP1, MIR4436B1, 34 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6627495copy number variation74nstd224human GRCh37 chr2: 110,863,908-110,983,320 , GRCh38.p12 chr2: 110,106,331-110,225,743 ACTR1AP1, MALL, 2 more genes
    nsv6627494copy number variation2nstd224human GRCh37 chr2: 110,482,930-110,983,320 , GRCh38.p12 chr2: 109,725,353-110,225,743 LOC440895, MIR4267, 22 more genes
    nsv6627492copy number variation1nstd224human GRCh37 chr2: 109,962,283-110,983,320 , GRCh38.p12 chr2: 109,345,827-110,225,743 GPAA1P1, RPL22P11, 29 more genes
    nsv6627308copy number variation1nstd224human GRCh37 chr2: 110,863,908-110,980,346 , GRCh38.p12 chr2: 110,106,331-110,222,769 MALL, MTLN, 2 more genes
    nsv6627307copy number variation1nstd224human GRCh37 chr2: 110,465,111-110,983,320 , GRCh38.p12 chr2: 109,707,534-110,225,743 RGPD5, LIMS3, 23 more genes
    nsv6627234copy number variation26nstd224human GRCh37 chr2: 110,852,875-110,983,320 , GRCh38.p12 chr2: 110,095,298-110,225,743 NPHP1, MALL, 2 more genes
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