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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6636272copy number variation1nstd102humanUncertain significance GRCh37 chr1: 172,399,416-172,468,762 , GRCh38.p12 chr1: 172,430,276-172,499,622 PIGC, LOC102724528, 1 more genes
    nsv4450997copy number variation1nstd102humanUncertain significance GRCh37 chr1: 172,362,787-172,508,698 , GRCh38.p12 chr1: 172,393,647-172,539,558 PIGC, C1orf105, 3 more genes
    nsv7095763copy number variation1nstd102humanUncertain significance GRCh37 chr1: 172,410,869-172,411,762 , GRCh38.p12 chr1: 172,441,729-172,442,622 PIGC, LOC102724528, 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 PIGC, CRB1, 1608 more genes
    nsv3874431copy number variation1nstd102humanPathogenic GRCh37 chr1: 171,990,029-195,086,758 , GRCh38.p12 chr1: 172,020,889-195,117,628 PIGC, PTGS2, 307 more genes
    nsv3873192copy number variation1nstd102humanPathogenic GRCh37 chr1: 161,676,893-184,071,723 , GRCh38.p12 chr1: 161,707,103-184,102,589 PIGC, COLGALT2, 402 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 PIGC, RPL18P2, 302 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 PIGC, RGSL1, 296 more genes
    nsv3889882copy number variation1nstd102humanPathogenic GRCh37 chr1: 159,815,642-177,026,983 , GRCh38.p12 chr1: 159,845,852-177,057,847 PIGC, FMO4, 403 more genes
    nsv4346684copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,369,890-175,796,325 , GRCh38.p12 chr1: 160,400,100-175,827,189 PIGC, LINC00626, 359 more genes
    nsv3901593copy number variation1nstd102humanPathogenic NCBI36 chr1: 161,618,937-174,112,781 , GRCh37 chr1: 163,352,313-175,846,158 , GRCh38 chr1: 163,382,523-175,877,022 PIGC, NME7, 233 more genes
    nsv3894431copy number variation1nstd102humanPathogenic NCBI36 chr1: 159,977,321-172,200,915 , GRCh37 chr1: 161,710,697-173,934,292 , GRCh38 chr1: 161,740,907-173,965,154 PIGC, RPL21P27, 238 more genes
    nsv3885424copy number variation1nstd102humanPathogenic GRCh37 chr1: 169,873,155-181,823,980 , GRCh38.p12 chr1: 169,904,014-181,854,845 PIGC, TRUND-NNN7-1, 210 more genes
    nsv3896314copy number variation1nstd102humanPathogenic GRCh37 chr1: 169,187,474-178,044,969 , NCBI36 chr1: 167,454,098-176,311,592 , GRCh38 chr1: 169,218,236-178,075,834 PIGC, RPS26P12, 150 more genes
    nsv3904950copy number variation1nstd102humanPathogenic GRCh38 chr1: 166,762,832-175,327,423 , NCBI36 chr1: 164,998,693-173,563,182 , GRCh37 chr1: 166,732,069-175,296,559 PIGC, LINC01681, 186 more genes
    nsv4674768copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,430,471-174,635,618 , GRCh38.p12 chr1: 167,461,234-174,666,480 PIGC, ATP1B1, 156 more genes
    nsv3893479copy number variation1nstd102humanPathogenic NCBI36 chr1: 166,550,684-173,535,058 , GRCh38 chr1: 168,314,822-175,299,299 , GRCh37 chr1: 168,284,060-175,268,435 PIGC, GORAB-AS1, 147 more genes
    nsv3885421copy number variation1nstd102humanPathogenic GRCh37 chr1: 169,095,250-175,778,910 , GRCh38.p12 chr1: 169,126,012-175,809,774 PIGC, ZBTB37, 130 more genes
    nsv6313519copy number variation1nstd102humanPathogenic GRCh37 chr1: 171,881,608-175,899,893 , GRCh38.p12 chr1: 171,912,468-175,930,757 PIGC, RNU6-693P, 73 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 PIGC, MARK1, 4930 more genes
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