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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5828705copy number variation1nstd209human GRCh38 chr1: 161,916,691-161,984,740 , GRCh37.p13 chr1: 161,886,481-161,954,530 ATF6, OLFML2B
    nsv5828074copy number variation1nstd209human GRCh38 chr1: 161,988,328-162,023,699 , GRCh37.p13 chr1: 161,958,118-161,993,489 OLFML2B
    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
    nsv4903970copy number variation1nstd200human GRCh38 chr1: 162,009,895-162,050,605 , GRCh37.p13 chr1: 161,979,685-162,020,395 OLFML2B
    nsv4897775copy number variation1nstd200human GRCh38 chr1: 162,022,547-162,025,679 , GRCh37.p13 chr1: 161,992,337-161,995,469 OLFML2B
    nsv4781239copy number variation1nstd200human GRCh37 chr1: 161,979,685-162,020,395 , GRCh38.p12 chr1: 162,009,895-162,050,605 OLFML2B
    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
    nsv4533617insertion1nstd166human GRCh37.p13 chr1: 161,954,137-161,954,137 , GRCh38.p12 chr1: 161,984,347-161,984,347 OLFML2B
    nsv4459312mobile element insertion1nstd166human GRCh37.p13 chr1: 161,973,886-161,973,886 , GRCh38.p12 chr1: 162,004,096-162,004,096 OLFML2B
    nsv4452657copy number variation1nstd102humanUncertain significance GRCh37 chr1: 160,744,174-162,583,871 , GRCh38.p12 chr1: 160,774,384-162,614,081 TRD-GTC2-2, KLHDC9, 104 more genes
    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
    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
    nsv4328159sequence alteration1nstd166human GRCh37.p13 chr1: 161,977,305-161,982,681 , GRCh38.p12 chr1: 162,007,515-162,012,891 OLFML2B
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
    nsv4319424inversion1nstd166human GRCh37.p13 chr1: 161,463,314-166,487,497 , GRCh38.p12 chr1: 161,493,524-166,518,260 , FCGR3B, 90 more genes
    nsv4059908copy number variation1nstd166human GRCh37.p13 chr1: 161,992,338-161,995,469 , GRCh38.p12 chr1: 162,022,548-162,025,679 OLFML2B
    nsv4053403copy number variation1nstd166human GRCh37.p13 chr1: 161,949,569-161,955,239 , GRCh38.p12 chr1: 161,979,779-161,985,449 OLFML2B
    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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