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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5432694copy number variation1nstd206human GRCh38 chr1: 42,690,525-42,690,648 , GRCh37.p13 chr1: 43,156,196-43,156,319 YBX1
    nsv4906163copy number variation1nstd200human GRCh38 chr1: 42,690,280-42,690,397 , GRCh37.p13 chr1: 43,155,951-43,156,068 YBX1
    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
    nsv4573519mobile element insertion1nstd166human GRCh37.p13 chr1: 43,152,904-43,152,904 , GRCh38.p12 chr1: 42,687,233-42,687,233 YBX1
    nsv4461908mobile element insertion1nstd166human GRCh37.p13 chr1: 43,169,539-43,169,539 , GRCh38.p12 chr1: 42,703,868-42,703,868 YBX1
    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
    nsv4326932inversion1nstd166human GRCh37.p13 chr1: 35,173,490-93,458,530 , GRCh38.p12 chr1: 34,707,889-92,992,973 , ATP6V0B, 1069 more genes
    nsv4051158copy number variation1nstd166human GRCh37.p13 chr1: 43,155,951-43,156,068 , GRCh38.p12 chr1: 42,690,280-42,690,397 YBX1
    nsv4047162copy number variation1nstd166human GRCh37.p13 chr1: 43,167,211-43,167,892 , GRCh38.p12 chr1: 42,701,540-42,702,221 YBX1
    nsv4035262copy number variation1nstd166human GRCh37.p13 chr1: 43,142,768-43,149,163 , GRCh38.p12 chr1: 42,677,097-42,683,492 PPIH, YBX1
    nsv3908884copy number variation1nstd102humanPathogenic GRCh37 chr1: 41,300,076-43,588,742 , GRCh38 chr1: 40,834,404-43,123,071 , NCBI36 chr1: 41,072,663-43,361,329 PPCS, ZNF691, 46 more genes
    nsv3900473copy number variation1nstd102humanPathogenic GRCh38 chr1: 40,693,289-44,514,104 , GRCh37 chr1: 41,158,961-44,979,776 , NCBI36 chr1: 40,931,548-44,752,363 KDM4A, RN7SL326P, 102 more genes
    nsv3892850copy number variation1nstd102humanLikely pathogenic NCBI36 chr1: 42,891,643-43,332,087 , GRCh37 chr1: 43,119,056-43,559,500 , GRCh38 chr1: 42,653,385-43,093,829 YBX1, SLC2A1, 17 more genes
    nsv3892747copy number variation1nstd102humanPathogenic NCBI36 chr1: 40,700,674-44,906,299 , GRCh37 chr1: 40,928,087-45,133,712 , GRCh38 chr1: 40,462,415-44,668,040 ERMAP, LOC100419796, 116 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 , SNAP47, 4927 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
    nsv3878135copy number variation1nstd102humanUncertain significance GRCh37 chr1: 33,241,563-46,663,513 , GRCh38.p12 chr1: 32,775,962-46,197,841 LINC02786, LOC105378678, 365 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 , MARK1, 4930 more genes
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