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Items: 1 to 20 of 273

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966091insertion1nstd209human GRCh38 chr2: 171,976,066-171,976,066 , GRCh37.p13 chr2: 172,832,578-172,832,578 HAT1
    nsv5901329copy number variation1nstd209human GRCh38 chr2: 171,953,200-171,955,466 , GRCh37.p13 chr2: 172,809,718-172,811,987 HAT1
    nsv5898527copy number variation1nstd209human GRCh38 chr2: 171,948,766-171,952,607 , GRCh37.p13 chr2: 172,805,286-172,809,125 HAT1
    nsv5894530copy number variation1nstd209human GRCh38 chr2: 171,962,979-171,963,036 , GRCh37.p13 chr2: 172,819,501-172,819,558 HAT1
    nsv5893400copy number variation1nstd209human GRCh38 chr2: 171,976,903-171,977,203 , GRCh37.p13 chr2: 172,841,842-172,842,142 HAT1
    nsv5832011copy number variation1nstd209human GRCh38 chr2: 171,953,083-171,955,483 , GRCh37.p13 chr2: 172,809,601-172,812,004 HAT1
    nsv5831742copy number variation1nstd209human GRCh38 chr2: 171,943,814-171,949,035 , GRCh37.p13 chr2: 172,800,333-172,805,555 HAT1
    nsv5831436copy number variation1nstd209human GRCh38 chr2: 171,921,232-171,942,036 , GRCh37.p13 chr2: 172,777,742-172,798,556 HAT1, LOC105373740
    nsv5718667mobile element insertion1nstd211human GRCh38 chr2: 171,930,931-171,930,931 , GRCh37.p13 chr2: 172,787,441-172,787,441 HAT1
    nsv5677799mobile element insertion1nstd211human GRCh38 chr2: 171,977,579-171,977,579 , GRCh37.p13 chr2: 172,842,488-172,842,488 HAT1
    nsv5623164insertion1nstd207human GRCh38 chr2: 171,976,066-171,976,066 , GRCh37.p13 chr2: 172,832,578-172,832,578 HAT1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5552191insertion1nstd206human GRCh38 chr2: 171,976,066-171,976,066 , GRCh37.p13 chr2: 172,832,578-172,832,578 HAT1
    nsv5449905copy number variation1nstd206human GRCh38 chr2: 171,921,290-171,921,347 , GRCh37.p13 chr2: 172,777,800-172,777,857 HAT1, LOC105373740
    nsv5446095copy number variation1nstd206human GRCh38 chr2: 171,977,538-171,977,857 , GRCh37.p13 chr2: 172,842,477-172,842,766 HAT1
    nsv5440056copy number variation1nstd206human GRCh38 chr2: 171,949,384-171,950,660 , GRCh37.p13 chr2: 172,805,904-172,807,179 HAT1
    nsv5439934copy number variation1nstd206human GRCh38 chr2: 171,972,143-171,972,193 , GRCh37.p13 chr2: 172,828,652-172,828,702 HAT1, LOC100420002
    nsv5437459copy number variation1nstd206human GRCh38 chr2: 171,953,215-171,955,454 , GRCh37.p13 chr2: 172,809,733-172,811,975 HAT1
    nsv5381341copy number variation1nstd102humanPathogenic GRCh37 chr2: 171,999,572-182,774,361 , GRCh38.p12 chr2: 171,143,062-181,909,634 ALDH7A1P2, LOC101927055, 174 more genes
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