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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099219copy number variation1nstd231human GRCh38.p12 chr1: 99,594,616-101,416,026 , GRCh37 chr1: 100,060,172-101,881,582 AGL, DBT, 38 more genes
    nsv7095681copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,316,599-101,709,564 , GRCh38.p12 chr1: 99,851,043-101,244,008 SLC35A3, S1PR1-DT, 29 more genes
    nsv7044488inversion1nstd229human GRCh38 chr1: 100,052,919-109,025,639 , GRCh37.p13 chr1: 100,518,475-109,568,261 LOC102723784, DNAJA1P5, 109 more genes
    nsv7038788inversion1nstd229human GRCh38 chr1: 100,641,361-100,847,342 , GRCh37.p13 chr1: 101,106,917-101,312,898 LINC01349, RPL36AP12, 1 more genes
    nsv6638177copy number variation1nstd229human GRCh38 chr1: 100,699,205-101,532,642 , GRCh37.p13 chr1: 101,164,761-101,998,198 S1PR1, LOC101928334, 11 more genes
    nsv6638109copy number variation1nstd229human GRCh38 chr1: 100,735,603-100,769,438 , GRCh37.p13 chr1: 101,201,159-101,234,994 VCAM1
    nsv6638108copy number variation1nstd229human GRCh38 chr1: 100,722,465-101,015,813 , GRCh37.p13 chr1: 101,188,021-101,481,369 DPH5, VCAM1, 3 more genes
    nsv6625469copy number variation1nstd224human GRCh37 chr1: 101,202,222-101,231,300 , GRCh38.p12 chr1: 100,736,666-100,765,744 VCAM1
    nsv6546790inversion1nstd223human GRCh38 chr1: 100,641,361-100,847,343 , GRCh37.p13 chr1: 101,106,917-101,312,899 VCAM1, LINC01349, 1 more genes
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
    nsv6290366copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,215,607-105,368,230 , GRCh38.p12 chr1: 99,750,051-104,825,608 LOC105379827, RPSAP19, 63 more genes
    nsv6133490copy number variation1nstd213human GRCh37 chr1: 101,020,000-101,380,001 , GRCh38.p12 chr1: 100,554,444-100,914,445 EXTL2, VCAM1, 4 more genes
    nsv5431577copy number variation1nstd206human GRCh38 chr1: 100,718,519-100,718,596 , GRCh37.p13 chr1: 101,184,075-101,184,152 VCAM1
    nsv5300062copy number variation1nstd204human GRCh38.p13 chr1: 100,676,555-100,800,956 , GRCh37.p13 chr1: 101,142,111-101,266,512 VCAM1
    nsv5201746copy number variation1nstd204human GRCh38.p13 chr1: 100,720,901-100,801,000 , GRCh37.p13 chr1: 101,186,457-101,266,556 VCAM1
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4745469copy number variation1nstd199human GRCh37 chr1: 86,005,697-146,486,085 , GRCh38.p12 chr1: 85,540,014-149,528,945 , TAF13, 920 more genes
    nsv4679627copy number variation1nstd189human GRCh37.p13 chr1: 100,661,887-101,495,928 , GRCh38.p12 chr1: 100,196,331-101,030,372 DBT, EXTL2, 18 more genes
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