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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099237copy number variation1nstd231human GRCh38.p12 chr1: 157,918,389-158,525,419 , GRCh37 chr1: 157,888,179-158,495,209 CD1A, CD1B, 24 more genes
    nsv7044121inversion1nstd229human GRCh38 chr1: 158,448,295-158,473,564 , GRCh37.p13 chr1: 158,418,085-158,443,354 OR10K1, EI24P2, 2 more genes
    nsv7041047inversion1nstd229human GRCh38 chr1: 154,596,558-159,585,927 , GRCh37.p13 chr1: 154,569,034-159,555,717 ADAR, SNORA80E, 204 more genes
    nsv7039558inversion1nstd229human GRCh38 chr1: 155,298,171-158,468,090 , GRCh37.p13 chr1: 155,267,962-158,437,880 FCRL4, SCARNA4, 121 more genes
    nsv6642593copy number variation1nstd229human GRCh38 chr1: 158,406,001-158,546,600 , GRCh37.p13 chr1: 158,375,791-158,516,390 OR10R2, OR6Y1, 9 more genes
    nsv6549694inversion1nstd223human GRCh38 chr1: 155,298,173-158,468,085 , GRCh37.p13 chr1: 155,267,964-158,437,875 ASH1L, GPATCH4, 121 more genes
    nsv6320339copy number variation1nstd223human GRCh38 chr1: 158,457,997-158,458,837 , GRCh37.p13 chr1: 158,427,787-158,428,627 LOC107985212
    nsv6225845insertion1nstd214human GRCh38 chr1: 158,462,370-158,462,370 , GRCh37.p13 chr1: 158,432,160-158,432,160 LOC107985212
    nsv6133742copy number variation1nstd213human GRCh37 chr1: 158,430,000-161,510,001 , GRCh38.p12 chr1: 158,460,210-161,540,211 APCS, FCER1A, 174 more genes
    nsv6133741copy number variation1nstd213human GRCh37 chr1: 158,390,000-161,480,001 , GRCh38.p12 chr1: 158,420,210-161,510,211 ATP1A4, CD48, 169 more genes
    nsv6133740copy number variation1nstd213human GRCh37 chr1: 158,330,000-161,530,001 , GRCh38.p12 chr1: 158,360,210-161,560,211 ATP1A2, ATP1A4, 178 more genes
    nsv6133563copy number variation1nstd213human GRCh37 chr1: 156,490,000-159,480,001 , GRCh38.p12 chr1: 156,520,208-159,510,211 CD1A, CD1D, 104 more genes
    nsv5964936insertion1nstd209human GRCh38 chr1: 158,462,370-158,462,370 , GRCh37.p13 chr1: 158,432,160-158,432,160 LOC107985212
    nsv5428618copy number variation1nstd206human GRCh38 chr1: 158,462,380-158,462,519 , GRCh37.p13 chr1: 158,432,170-158,432,309 LOC107985212
    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
    nsv5177643mobile element insertion1nstd203human GRCh38 chr1: 158,461,239-158,461,243 , GRCh37.p13 chr1: 158,431,029-158,431,033 LOC107985212
    nsv4784387copy number variation1nstd200human GRCh37 chr1: 158,431,727-158,437,465 , GRCh38.p12 chr1: 158,461,937-158,467,675 LOC107985212, OR10K1
    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
    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
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