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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096586copy number variation1nstd102humanUncertain significance GRCh37 chr2: 171,675,102-174,232,392 , GRCh38.p12 chr2: 170,818,592-173,367,664 RNU6-182P, DCAF17, 36 more genes
    nsv6688715copy number variation1nstd229human GRCh38 chr2: 172,041,314-172,045,517 , GRCh37.p13 chr2: 172,906,225-172,910,245 METAP1D
    nsv6679956copy number variation1nstd229human GRCh38 chr2: 172,005,450-172,017,305 , GRCh37.p13 chr2: 172,870,358-172,882,210 METAP1D
    nsv6679710copy number variation1nstd229human GRCh38 chr2: 171,996,549-172,001,370 , GRCh37.p13 chr2: 172,861,456-172,866,277 METAP1D
    nsv6551736inversion1nstd223human GRCh38 chr2: 172,068,264-172,068,805 , GRCh37.p13 chr2: 172,932,992-172,933,533 METAP1D
    nsv6547928inversion1nstd223human GRCh38 chr2: 172,032,897-172,033,530 , GRCh37.p13 chr2: 172,897,800-172,898,433 METAP1D
    nsv6546210inversion1nstd223human GRCh38 chr2: 172,029,115-172,030,068 , GRCh37.p13 chr2: 172,894,018-172,894,971 METAP1D
    nsv6545544inversion1nstd223human GRCh38 chr2: 172,015,006-172,015,642 , GRCh37.p13 chr2: 172,879,911-172,880,547 METAP1D
    nsv6544585inversion1nstd223human GRCh38 chr2: 172,040,788-172,041,375 , GRCh37.p13 chr2: 172,905,699-172,906,286 METAP1D
    nsv6541552inversion1nstd223human GRCh38 chr2: 172,068,327-172,068,805 , GRCh37.p13 chr2: 172,933,055-172,933,533 METAP1D
    nsv6541214inversion1nstd223human GRCh38 chr2: 172,059,149-172,059,922 , GRCh37.p13 chr2: 172,923,877-172,924,650 METAP1D
    nsv6353752copy number variation1nstd223human GRCh38 chr2: 172,035,301-172,036,500 , GRCh37.p13 chr2: 172,900,204-172,901,404 METAP1D
    nsv6349092copy number variation1nstd223human GRCh38 chr2: 171,996,546-172,001,370 , GRCh37.p13 chr2: 172,861,453-172,866,277 METAP1D
    nsv6348097copy number variation1nstd223human GRCh38 chr2: 172,040,801-172,045,300 , GRCh37.p13 chr2: 172,905,712-172,910,028 METAP1D
    nsv6345928copy number variation1nstd223human GRCh38 chr2: 171,999,601-172,000,100 , GRCh37.p13 chr2: 172,864,508-172,865,007 METAP1D
    nsv6345554copy number variation1nstd223human GRCh38 chr2: 172,050,736-172,051,209 , GRCh37.p13 chr2: 172,915,464-172,915,937 METAP1D
    nsv6341812copy number variation1nstd223human GRCh38 chr2: 172,007,932-172,011,002 , GRCh37.p13 chr2: 172,872,837-172,875,909 METAP1D
    nsv6335772copy number variation1nstd223human GRCh38 chr2: 172,002,391-172,002,835 , GRCh37.p13 chr2: 172,867,299-172,867,743 METAP1D
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315160copy number variation1nstd102humanPathogenic GRCh37 chr2: 160,347,642-174,075,851 , GRCh38.p12 chr2: 159,491,131-173,211,123 EIF3EP3, FAP, 158 more genes
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