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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5212241copy number variation1nstd204human GRCh38.p13 chr1: 28,084,401-28,971,400 , GRCh37.p13 chr1: 28,410,912-29,297,912 SNORA73B, ARL8BP2, 29 more genes
    nsv5201536copy number variation1nstd204human GRCh37.p13 chr1: 28,803,613-28,860,312 , GRCh38.p13 chr1: 28,477,101-28,533,800 RCC1, SNORA73A, 5 more genes
    nsv4903278copy number variation1nstd200human GRCh38 chr1: 28,479,032-28,481,731 , GRCh37.p13 chr1: 28,805,544-28,808,243 PHACTR4, RNU6ATAC27P
    nsv4895614copy number variation1nstd200human GRCh38 chr1: 28,479,402-28,479,591 , GRCh37.p13 chr1: 28,805,914-28,806,103 PHACTR4, RNU6ATAC27P
    nsv4895612copy number variation1nstd200human GRCh38 chr1: 28,433,847-28,481,925 , GRCh37.p13 chr1: 28,760,358-28,808,437 PHACTR4, RNU6ATAC27P
    nsv4780738copy number variation1nstd200human GRCh37 chr1: 28,805,544-28,808,243 , GRCh38.p12 chr1: 28,479,032-28,481,731 PHACTR4, RNU6ATAC27P
    nsv4780737copy number variation1nstd200human GRCh37 chr1: 28,795,142-28,905,455 , GRCh38.p12 chr1: 28,468,631-28,578,943 RNU6ATAC27P, SNORA73A, 11 more genes
    nsv4772819copy number variation1nstd200human GRCh37 chr1: 28,760,358-28,808,437 , GRCh38.p12 chr1: 28,433,847-28,481,925 RNU6ATAC27P, PHACTR4
    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
    nsv4594454copy number variation1nstd183human GRCh37 chr1: 28,284,815-28,955,102 , GRCh38.p12 chr1: 27,958,304-28,628,590 RNU6ATAC27P, ARL8BP2, 26 more genes
    nsv4580975copy number variation1nstd183human GRCh37 chr1: 28,624,481-28,943,345 , GRCh38.p12 chr1: 28,297,970-28,616,833 SNHG12, TRNAU1AP, 14 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv3918127copy number variation1nstd102humanUncertain significance NCBI36 chr1: 28,645,394-28,806,136 , GRCh37.p13 chr1: 28,772,807-28,933,549 , GRCh38.p12 chr1: 28,446,296-28,607,037 TAF12, SNHG12, 13 more genes
    nsv3909774copy number variation1nstd102humanUncertain significance NCBI36 chr1: 28,497,755-28,833,661 , GRCh37 chr1: 28,625,168-28,961,074 , GRCh38 chr1: 28,298,657-28,634,562 SNORA16A, SNORA61, 14 more genes
    nsv3907483copy number variation1nstd102humanPathogenic GRCh37 chr1: 27,289,536-32,744,646 , GRCh38 chr1: 26,963,045-32,279,045 , NCBI36 chr1: 27,162,123-32,517,233 ATP5IF1, LOC102723760, 138 more genes
    nsv3901163copy number variation1nstd102humanPathogenic GRCh37 chr1: 24,707,696-41,886,350 , GRCh38 chr1: 24,381,206-41,401,517 , NCBI36 chr1: 24,580,283-41,658,937 TMEM222, ZBTB8OS, 453 more genes
    nsv3894712copy number variation1nstd102humanUncertain significance GRCh37 chr1: 28,245,710-28,933,738 , GRCh38 chr1: 27,919,199-28,607,226 , NCBI36 chr1: 28,118,297-28,806,325 SNHG12, TRNAU1AP, 26 more genes
    nsv3891425copy number variation1nstd102humanPathogenic NCBI36 chr1: 28,623,965-33,361,042 , GRCh37 chr1: 28,751,378-33,588,455 , GRCh38 chr1: 28,424,867-33,122,854 SNHG3, LOC105378620, 115 more genes
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