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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
    nsv5872402copy number variation1nstd209human GRCh38 chr1: 25,822,448-25,822,773 , GRCh37.p13 chr1: 26,148,939-26,149,264 MTFR1L, LOC646471
    nsv5673254copy number variation1nstd102humanPathogenic GRCh37 chr1: 25,870,180-26,795,632 , GRCh38.p12 chr1: 25,543,689-26,469,141 LDLRAP1, AUNIP, 36 more genes
    nsv5569217copy number variation1nstd207human GRCh38 chr1: 25,822,448-25,822,773 , GRCh37.p13 chr1: 26,148,939-26,149,264 MTFR1L, LOC646471
    nsv5428624copy number variation1nstd206human GRCh38 chr1: 25,819,437-25,819,505 , GRCh37.p13 chr1: 26,145,928-26,145,996 MTFR1L, LOC646471
    nsv5427686copy number variation1nstd206human GRCh38 chr1: 22,064,395-28,290,354 , GRCh37.p13 chr1: 22,390,888-28,616,865 , NCMAP-DT, 201 more genes
    nsv5420696copy number variation1nstd206human GRCh38 chr1: 25,821,664-25,822,766 , GRCh37.p13 chr1: 26,148,155-26,149,257 MTFR1L, LOC646471
    nsv5415690copy number variation1nstd206human GRCh38 chr1: 25,822,450-25,822,774 , GRCh37.p13 chr1: 26,148,941-26,149,265 MTFR1L, LOC646471
    nsv5385137copy number variation2nstd186human GRCh37 chr1: 26,148,941-26,149,265 , GRCh38.p12 chr1: 25,822,450-25,822,774 MTFR1L, LOC646471
    nsv5285916copy number variation1nstd204human GRCh37.p13 chr1: 26,148,937-26,149,273 , GRCh38.p13 chr1: 25,822,446-25,822,782 MTFR1L, LOC646471
    nsv4895450copy number variation1nstd200human GRCh38 chr1: 25,822,450-25,822,774 , GRCh37.p13 chr1: 26,148,941-26,149,265 MTFR1L, LOC646471
    nsv4895449copy number variation1nstd200human GRCh38 chr1: 25,813,969-25,822,360 , GRCh37.p13 chr1: 26,140,460-26,148,851 LOC646471, SELENON, 1 more genes
    nsv4788547copy number variation1nstd200human GRCh37 chr1: 26,148,941-26,149,265 , GRCh38.p12 chr1: 25,822,450-25,822,774 MTFR1L, LOC646471
    nsv4788546copy number variation1nstd200human GRCh37 chr1: 26,140,460-26,148,851 , GRCh38.p12 chr1: 25,813,969-25,822,360 SELENON, LOC646471, 1 more genes
    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
    nsv4713918copy number variation1nstd195human GRCh37 chr1: 26,148,939-26,148,940 , GRCh38.p12 chr1: 25,822,448-25,822,449 MTFR1L, LOC646471
    nsv4684184copy number variation1nstd102humanUncertain significance GRCh37 chr1: 25,872,197-26,274,156 , GRCh38.p12 chr1: 25,545,706-25,947,665 MAN1C1, MTFR1L, 10 more genes
    nsv4647294copy number variation1nstd186human GRCh37 chr1: 26,148,941-26,149,361 , GRCh38.p12 chr1: 25,822,450-25,822,870 MTFR1L, LOC646471
    nsv4645449mobile element deletion1nstd186human GRCh37 chr1: 26,148,940-26,149,265 , GRCh38.p12 chr1: 25,822,449-25,822,774 MTFR1L, LOC646471
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