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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5214874copy number variation1nstd204human GRCh38.p13 chr1: 110,085,896-110,088,795 , GRCh37.p13 chr1: 110,628,518-110,631,417 LINC01397
    nsv4890737copy number variation1nstd200human GRCh38 chr1: 110,106,541-110,106,676 , GRCh37.p13 chr1: 110,649,163-110,649,298 LINC01397
    nsv4890736copy number variation1nstd200human GRCh38 chr1: 110,095,602-110,096,553 , GRCh37.p13 chr1: 110,638,224-110,639,175 LINC01397
    nsv4890735copy number variation1nstd200human GRCh38 chr1: 110,083,210-110,084,793 , GRCh37.p13 chr1: 110,625,832-110,627,415 LINC01397
    nsv4890734copy number variation1nstd200human GRCh38 chr1: 110,082,897-110,083,053 , GRCh37.p13 chr1: 110,625,519-110,625,675 LINC01397
    nsv4773644copy number variation1nstd200human GRCh37 chr1: 110,649,163-110,649,298 , GRCh38.p12 chr1: 110,106,541-110,106,676 LINC01397
    nsv4773643copy number variation1nstd200human GRCh37 chr1: 110,638,224-110,639,175 , GRCh38.p12 chr1: 110,095,602-110,096,553 LINC01397
    nsv4773642copy number variation1nstd200human GRCh37 chr1: 110,625,519-110,625,675 , GRCh38.p12 chr1: 110,082,897-110,083,053 LINC01397
    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
    nsv4453642copy number variation1nstd102humannot provided GRCh37 chr1: 108,926,313-111,266,497 , GRCh38.p12 chr1: 108,383,691-110,723,875 PSMA5, GSTM1, 79 more genes
    nsv4436700copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 107,779,092-111,199,205 , GRCh38.p12 chr1: 107,236,470-110,656,583 ALX3, AMPD2, 89 more genes
    nsv4330538inversion1nstd166human GRCh37.p13 chr1: 94,223,082-113,632,613 , GRCh38.p12 chr1: 93,757,526-113,089,991 , AMPD2, 329 more genes
    nsv4065824copy number variation1nstd166human GRCh37.p13 chr1: 110,625,832-110,627,415 , GRCh38.p12 chr1: 110,083,210-110,084,793 LINC01397
    nsv4056937copy number variation1nstd166human GRCh37.p13 chr1: 110,625,519-110,625,675 , GRCh38.p12 chr1: 110,082,897-110,083,053 LINC01397
    nsv3966563insertion1nstd168human GRCh38 chr1: 110,064,401-110,143,423 , GRCh37.p13 chr1: 110,607,023-110,686,045 ALX3, UBL4B, 1 more genes
    nsv3963233complex substitution1nstd168human GRCh38 chr1: 110,101,997-110,122,558 , GRCh37.p13 chr1: 110,644,619-110,665,180 UBL4B, LINC01397
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