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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3880581copy number variation1nstd102humanBenign GRCh37 chr1: 186,304,298-186,425,526 , GRCh38.p12 chr1: 186,335,166-186,456,394 TPR, PDC, 2 more genes
    nsv3887784copy number variation1nstd102humanBenign GRCh37 chr1: 186,281,328-186,390,303 , GRCh38.p12 chr1: 186,312,196-186,421,171 TPR, RNU6-1240P, 2 more genes
    nsv3876180copy number variation1nstd102humanBenign GRCh37 chr1: 186,280,235-186,382,460 , GRCh38.p12 chr1: 186,311,103-186,413,328 TPR, ODR4, 2 more genes
    nsv4453775copy number variation1nstd102humanUncertain significance GRCh37 chr1: 186,318,114-186,573,823 , GRCh38.p12 chr1: 186,348,982-186,604,691 TPR, LOC100131939, 3 more genes
    nsv3901971copy number variation1nstd102humanUncertain significance GRCh38 chr1: 186,356,477-186,580,632 , GRCh37 chr1: 186,325,609-186,549,764 , NCBI36 chr1: 184,592,232-184,816,387 TPR, ODR4, 3 more genes
    nsv3870852copy number variation1nstd102humanUncertain significance GRCh37 chr1: 186,328,876-186,430,216 , GRCh38.p12 chr1: 186,359,744-186,461,084 TPR, ODR4, 2 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 TPR, CRB1, 1608 more genes
    nsv3874431copy number variation1nstd102humanPathogenic GRCh37 chr1: 171,990,029-195,086,758 , GRCh38.p12 chr1: 172,020,889-195,117,628 TPR, PTGS2, 307 more genes
    nsv3888143copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,413,479-201,764,737 , GRCh38.p12 chr1: 179,444,344-201,795,609 TPR, CSRP1-AS1, 273 more genes
    nsv4673925copy number variation1nstd102humanPathogenic GRCh37 chr1: 177,551,193-199,599,056 , GRCh38.p12 chr1: 177,582,058-199,629,928 TPR, QSOX1, 263 more genes
    nsv3878624copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,073,386-200,192,265 , GRCh38.p12 chr1: 179,104,251-200,223,137 TPR, LOC105371661, 249 more genes
    nsv3905741copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,002,040-199,694,025 , NCBI36 chr1: 177,268,663-197,960,648 , GRCh38 chr1: 179,032,905-199,724,897 TPR, SLC4A1APP2, 240 more genes
    nsv3904393copy number variation1nstd102humanPathogenic GRCh37 chr1: 170,898,861-191,034,539 , GRCh38 chr1: 170,929,720-191,065,409 , NCBI36 chr1: 169,165,485-189,301,162 TPR, RPL18P2, 302 more genes
    nsv3877653copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,011,314-199,022,759 , GRCh38.p12 chr1: 179,042,179-199,053,630 TPR, LINC02818, 234 more genes
    nsv3896481copy number variation1nstd102humanPathogenic GRCh38 chr1: 176,595,962-196,301,688 , GRCh37 chr1: 176,565,098-196,270,818 , NCBI36 chr1: 174,831,721-194,537,441 TPR, RN7SL230P, 231 more genes
    nsv3901149copy number variation1nstd102humanPathogenic NCBI36 chr1: 168,271,833-185,790,903 , GRCh37 chr1: 170,005,209-187,524,280 , GRCh38 chr1: 170,036,068-187,555,148 TPR, RGSL1, 296 more genes
    nsv3886667copy number variation1nstd102humanPathogenic GRCh37 chr1: 173,131,908-187,406,532 , GRCh38.p12 chr1: 173,162,769-187,437,400 TPR, CRYZL2P, 233 more genes
    nsv6637124copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,727,182-192,260,142 , GRCh38.p12 chr1: 179,758,047-192,291,012 TPR, LOC101928933, 148 more genes
    nsv6290451copy number variation1nstd102humanPathogenic GRCh37 chr1: 178,522,021-190,322,133 , GRCh38.p12 chr1: 178,552,886-190,353,003 TPR, RNU7-13P, 167 more genes
    nsv3872146copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,572,003-191,524,283 , GRCh38.p12 chr1: 181,602,867-191,555,153 TPR, PLA2G4A, 110 more genes
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