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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5037746inversion1nstd200human GRCh38 chr1: 95,317,720-95,774,567 , GRCh37.p13 chr1: 95,783,276-96,240,123 LINC01761, LINC01760, 6 more genes
    nsv4897074copy number variation1nstd200human GRCh38 chr1: 95,512,681-95,524,708 , GRCh37.p13 chr1: 95,978,237-95,990,264 LINC02607
    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
    nsv4674663copy number variation1nstd102humanUncertain significance GRCh37 chr1: 93,863,518-96,108,930 , GRCh38.p12 chr1: 93,397,961-95,643,374 CNN3, SLC44A3-AS1, 48 more genes
    nsv4583111copy number variation1nstd183human GRCh37 chr1: 95,939,767-96,013,733 , GRCh38.p12 chr1: 95,474,211-95,548,177 LINC02607, LINC01761
    nsv4517071copy number variation1nstd166human GRCh37.p13 chr1: 95,796,998-96,112,000 , GRCh38.p12 chr1: 95,331,442-95,646,444 LOC107985420, LOC101928219, 3 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
    nsv4330538inversion1nstd166human GRCh37.p13 chr1: 94,223,082-113,632,613 , GRCh38.p12 chr1: 93,757,526-113,089,991 , AMPD2, 329 more genes
    nsv4065161copy number variation1nstd166human GRCh37.p13 chr1: 95,974,933-95,975,023 , GRCh38.p12 chr1: 95,509,377-95,509,467 LINC02607
    nsv3898327copy number variation1nstd102humanPathogenic GRCh38 chr1: 83,457,325-104,273,917 , GRCh37 chr1: 83,923,008-104,816,539 , NCBI36 chr1: 83,695,596-104,618,062 LINC01773, LOC107985095, 322 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 , SNAP47, 4927 more genes
    nsv3884558copy number variation1nstd102humanPathogenic GRCh37 chr1: 94,054,724-111,671,707 , GRCh38.p12 chr1: 93,589,167-111,129,085 SLC25A24, LOC100271656, 265 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 , RNU1-153P, 4887 more genes
    nsv3882833copy number variation1nstd102humanUncertain significance GRCh37 chr1: 95,554,116-96,359,492 , GRCh38.p12 chr1: 95,088,560-95,893,936 LINC02607, TLCD4, 10 more genes
    nsv3882464copy number variation1nstd102humanPathogenic GRCh37 chr1: 93,837,992-121,343,783 , GRCh38.p12 chr1: 93,372,435-121,601,985 LINC02607, RNVU1-19, 513 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 , MARK1, 4930 more genes
    nsv3873984copy number variation1nstd102humanBenign GRCh37 chr1: 95,766,707-96,143,770 , GRCh38.p12 chr1: 95,301,151-95,678,214 LINC01760, LOC101928219, 6 more genes
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