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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5724763mobile element insertion1nstd211human GRCh38 chr1: 160,608,909-160,608,909 , GRCh37.p13 chr1: 160,578,699-160,578,699 SLAMF1
    nsv5557747mobile element insertion1nstd206human GRCh38 chr1: 160,608,924-160,608,960 , GRCh37.p13 chr1: 160,578,714-160,578,750 SLAMF1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5200016mobile element insertion1nstd203human GRCh38 chr1: 160,608,909-160,608,924 , GRCh37.p13 chr1: 160,578,699-160,578,714 SLAMF1
    nsv5075880mobile element insertion1nstd203human GRCh38 chr1: 160,621,269-160,621,280 , GRCh37.p13 chr1: 160,591,059-160,591,070 SLAMF1
    nsv4903958copy number variation1nstd200human GRCh38 chr1: 160,628,311-160,628,614 , GRCh37.p13 chr1: 160,598,101-160,598,404 SLAMF1
    nsv4781232copy number variation1nstd200human GRCh37 chr1: 160,598,101-160,598,404 , GRCh38.p12 chr1: 160,628,311-160,628,614 SLAMF1
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4579409copy number variation1nstd183human GRCh37 chr1: 160,602,909-160,712,928 , GRCh38.p12 chr1: 160,633,119-160,743,138 SLAMF1, SETP9, 3 more genes
    nsv4459037mobile element insertion1nstd166human GRCh37.p13 chr1: 160,579,808-160,579,808 , GRCh38.p12 chr1: 160,610,018-160,610,018 SLAMF1
    nsv4450412copy number variation1nstd102humanPathogenic GRCh37 chr1: 157,321,299-167,391,423 , GRCh38.p12 chr1: 157,351,509-167,422,186 FCGR3B, SLAMF9, 302 more genes
    nsv4450321copy number variation1nstd102humanUncertain significance GRCh37 chr1: 159,808,188-161,011,163 , GRCh38.p12 chr1: 159,838,398-161,041,373 LOC107985216, PPIAP37, 50 more genes
    nsv4346684copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,369,890-175,796,325 , GRCh38.p12 chr1: 160,400,100-175,827,189 LINC00626, RN7SL861P, 359 more genes
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
    nsv4062869copy number variation1nstd166human GRCh37.p13 chr1: 160,607,723-160,607,854 , GRCh38.p12 chr1: 160,637,933-160,638,064 SLAMF1
    nsv4060564copy number variation1nstd166human GRCh37.p13 chr1: 160,610,579-160,610,634 , GRCh38.p12 chr1: 160,640,789-160,640,844 SLAMF1
    nsv3968826copy number variation1nstd168human GRCh38 chr1: 160,566,114-160,608,257 , GRCh37.p13 chr1: 160,535,904-160,578,047 CD84, SLAMF1, 1 more genes
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , LOC101060227, 1608 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , CRB1, 1608 more genes
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