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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5880990copy number variation1nstd209human GRCh38 chr1: 863,087-962,195 , GRCh37.p13 chr1: 798,467-897,575 NOC2L, SAMD11, 7 more genes
    nsv5869149copy number variation1nstd209human GRCh38 chr1: 858,988-929,734 , GRCh37.p13 chr1: 794,368-865,114 SAMD11, FAM41C, 6 more genes
    nsv5830827copy number variation3nstd209human GRCh38 chr1: 866,846-872,451 , GRCh37.p13 chr1: 802,226-807,831 TUBB8P11, FAM41C, 1 more genes
    nsv5830786copy number variation3nstd209human GRCh38 chr1: 876,508-878,797 , GRCh37.p13 chr1: 811,888-814,177 FAM41C
    nsv5830684copy number variation3nstd209human GRCh38 chr1: 860,868-875,657 , GRCh37.p13 chr1: 796,248-811,037 TUBB8P11, FAM41C, 1 more genes
    nsv5830523copy number variation3nstd209human GRCh38 chr1: 872,899-875,807 , GRCh37.p13 chr1: 808,279-811,187 TUBB8P11, FAM41C
    nsv5729972mobile element insertion1nstd211human GRCh38 chr1: 868,485-868,485 , GRCh37.p13 chr1: 803,865-803,865 LOC107984850, FAM41C
    nsv5726959mobile element insertion2nstd211human GRCh38 chr1: 876,902-876,902 , GRCh37.p13 chr1: 812,282-812,282 FAM41C
    nsv5682752mobile element insertion1nstd211human GRCh38 chr1: 866,135-866,135 , GRCh37.p13 chr1: 801,515-801,515 FAM41C, LOC107984850
    nsv5624193insertion1nstd207human GRCh38 chr1: 876,024-876,024 , GRCh37.p13 chr1: 811,404-811,404 FAM41C
    nsv5623672insertion1nstd207human GRCh38 chr1: 876,247-876,247 , GRCh37.p13 chr1: 811,627-811,627 FAM41C
    nsv5623257insertion1nstd207human GRCh38 chr1: 866,851-866,851 , GRCh37.p13 chr1: 802,231-802,231 LOC107984850, FAM41C
    nsv5623243insertion1nstd207human GRCh38 chr1: 866,559-866,559 , GRCh37.p13 chr1: 801,939-801,939 LOC107984850, FAM41C
    nsv5617022insertion2nstd207human GRCh38 chr1: 872,566-872,566 , GRCh37.p13 chr1: 807,946-807,946 FAM41C, TUBB8P11
    nsv5616950insertion1nstd207human GRCh38 chr1: 872,840-872,840 , GRCh37.p13 chr1: 808,220-808,220 FAM41C, TUBB8P11
    nsv5614463insertion1nstd207human GRCh38 chr1: 872,986-872,986 , GRCh37.p13 chr1: 808,366-808,366 TUBB8P11, FAM41C
    nsv5609428insertion1nstd207human GRCh38 chr1: 876,300-876,300 , GRCh37.p13 chr1: 811,680-811,680 FAM41C
    nsv5606364insertion1nstd207human GRCh38 chr1: 868,470-868,470 , GRCh37.p13 chr1: 803,850-803,850 FAM41C, LOC107984850
    nsv5606179insertion2nstd207human GRCh38 chr1: 876,014-876,014 , GRCh37.p13 chr1: 811,394-811,394 FAM41C
    nsv5581718copy number variation1nstd207human GRCh38 chr1: 872,669-872,878 , GRCh37.p13 chr1: 808,049-808,258 FAM41C, TUBB8P11
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