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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963464insertion1nstd209human GRCh38 chr1: 778,706-778,706 , GRCh37.p13 chr1: 714,086-714,086 LINC01409, LOC100288069
    nsv5830762copy number variation3nstd209human GRCh38 chr1: 810,029-820,325 , GRCh37.p13 chr1: 745,409-755,705 FAM87B, LINC01409
    nsv5830757copy number variation4nstd209human GRCh38 chr1: 791,761-799,262 , GRCh37.p13 chr1: 727,141-734,642 LINC01409
    nsv5830756copy number variation4nstd209human GRCh38 chr1: 777,535-788,739 , GRCh37.p13 chr1: 712,915-724,119 LOC100288069, LINC01409
    nsv5830657copy number variation3nstd209human GRCh38 chr1: 802,408-810,831 , GRCh37.p13 chr1: 737,788-746,211 LINC01409
    nsv5830654copy number variation4nstd209human GRCh38 chr1: 793,039-805,671 , GRCh37.p13 chr1: 728,419-741,051 LINC01409
    nsv5830477copy number variation3nstd209human GRCh38 chr1: 800,201-806,954 , GRCh37.p13 chr1: 735,581-742,334 LINC01409
    nsv5830167copy number variation3nstd209human GRCh38 chr1: 808,716-813,699 , GRCh37.p13 chr1: 744,096-749,079 LINC01409
    nsv5830159copy number variation3nstd209human GRCh38 chr1: 802,407-807,437 , GRCh37.p13 chr1: 737,787-742,817 LINC01409
    nsv5830156copy number variation5nstd209human GRCh38 chr1: 791,760-798,021 , GRCh37.p13 chr1: 727,140-733,401 LINC01409
    nsv5609461insertion1nstd207human GRCh38 chr1: 795,574-795,574 , GRCh37.p13 chr1: 730,954-730,954 LINC01409
    nsv5604957insertion1nstd207human GRCh38 chr1: 789,481-789,481 , GRCh37.p13 chr1: 724,861-724,861 LINC01409
    nsv5432017copy number variation1nstd206human GRCh38 chr1: 803,230-806,636 , GRCh37.p13 chr1: 738,610-742,016 LINC01409
    nsv5423417copy number variation1nstd206human GRCh38 chr1: 778,728-778,780 , GRCh37.p13 chr1: 714,108-714,160 LINC01409, LOC100288069
    nsv5422961copy number variation1nstd206human GRCh38 chr1: 731,650-915,000 , GRCh37.p13 chr1: 667,030-850,380 FAM87B, LINC02593, 9 more genes
    nsv5421839copy number variation1nstd206human GRCh38 chr1: 793,973-893,064 , GRCh37.p13 chr1: 729,353-828,444 LINC00115, FAM41C, 5 more genes
    nsv5344223translocation1nstd200human GRCh37 chr1: 761,226-761,226 , GRCh37 chr1: 729,346-729,346 , GRCh38.p12 chr1: 793,966-793,966 , GRCh38.p12 chr1: 825,846-825,846 LINC00115, LINC01128, 1 more genes
    nsv5321650translocation1nstd204human GRCh38.p13 chr1: 793,966-793,966 , GRCh38.p13 chr1: 825,846-825,846 , GRCh37.p13 chr1: 729,346-729,346 , GRCh37.p13 chr1: 761,226-761,226 LINC00115, LINC01128, 1 more genes
    nsv5219268copy number variation1nstd204human GRCh38.p13 chr1: 791,206-793,545 , GRCh37.p13 chr1: 726,586-728,925 LINC01409
    nsv5218990copy number variation1nstd204human GRCh38.p13 chr1: 792,589-822,462 , GRCh37.p13 chr1: 727,969-757,842 LINC01409, FAM87B
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