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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126162insertion1nstd186human GRCh37 chr1: 151,741,762-151,741,762 , GRCh38.p12 chr1: 151,769,286-151,769,286 OAZ3, TDRKH
    nsv5964724insertion1nstd209human GRCh38 chr1: 151,769,286-151,769,286 , GRCh37.p13 chr1: 151,741,762-151,741,762 TDRKH, OAZ3
    nsv5687204mobile element insertion1nstd211human GRCh38 chr1: 151,789,366-151,789,366 , GRCh37.p13 chr1: 151,761,842-151,761,842 TDRKH, TDRKH-AS1
    nsv5621613insertion1nstd207human GRCh38 chr1: 151,769,286-151,769,286 , GRCh37.p13 chr1: 151,741,762-151,741,762 OAZ3, TDRKH
    nsv5550766insertion1nstd206human GRCh38 chr1: 151,769,286-151,769,286 , GRCh37.p13 chr1: 151,741,762-151,741,762 TDRKH, OAZ3
    nsv5431964copy number variation1nstd206human GRCh38 chr1: 151,785,089-151,795,158 , GRCh37.p13 chr1: 151,757,565-151,767,634 TDRKH, TDRKH-AS1
    nsv5427814copy number variation1nstd206human GRCh38 chr1: 151,776,694-151,776,926 , GRCh37.p13 chr1: 151,749,170-151,749,402 TDRKH, LOC100270670
    nsv5415434copy number variation1nstd206human GRCh38 chr1: 151,788,398-151,788,467 , GRCh37.p13 chr1: 151,760,874-151,760,943 TDRKH
    nsv5395631mobile element insertion1nstd206human GRCh38 chr1: 151,789,366-151,789,417 , GRCh37.p13 chr1: 151,761,842-151,761,893 TDRKH-AS1, TDRKH
    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
    nsv5280724copy number variation1nstd204human GRCh38.p13 chr1: 151,765,478-151,773,413 , GRCh37.p13 chr1: 151,737,954-151,745,889 TDRKH, OAZ3
    nsv5212146copy number variation1nstd204human GRCh38.p13 chr1: 151,765,376-151,773,074 , GRCh37.p13 chr1: 151,737,852-151,745,550 OAZ3, TDRKH
    nsv5077093mobile element insertion1nstd203human GRCh38 chr1: 151,773,638-151,773,647 , GRCh37.p13 chr1: 151,746,114-151,746,123 TDRKH
    nsv5076179mobile element insertion1nstd203human GRCh38 chr1: 151,772,280-151,772,282 , GRCh37.p13 chr1: 151,744,756-151,744,758 TDRKH
    nsv4903858copy number variation1nstd200human GRCh38 chr1: 151,765,692-151,773,210 , GRCh37.p13 chr1: 151,738,168-151,745,686 TDRKH, OAZ3
    nsv4897390copy number variation1nstd200human GRCh38 chr1: 151,777,391-151,781,203 , GRCh37.p13 chr1: 151,749,867-151,753,679 TDRKH, LOC100270670
    nsv4784215copy number variation1nstd200human GRCh37 chr1: 151,749,867-151,753,679 , GRCh38.p12 chr1: 151,777,391-151,781,203 LOC100270670, TDRKH
    nsv4781187copy number variation1nstd200human GRCh37 chr1: 151,738,188-151,745,662 , GRCh38.p12 chr1: 151,765,712-151,773,186 TDRKH, OAZ3
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4758017insertion1nstd199human GRCh37 chr1: 151,741,720-151,741,720 , GRCh38.p12 chr1: 151,769,244-151,769,244 TDRKH, OAZ3
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