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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096653copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,121,051-47,710,088 , GRCh38.p12 chr2: 37,893,908-47,482,949 PLEKHH2, RNU6-566P, 151 more genes
    nsv7096652copy number variation1nstd102humanPathogenic GRCh37 chr2: 37,334,416-39,347,563 , GRCh38.p12 chr2: 37,107,273-39,120,422 RPL31P16, GALM, 52 more genes
    nsv6661709copy number variation1nstd229human GRCh38 chr2: 38,775,005-38,992,126 , GRCh37.p13 chr2: 39,002,147-39,219,267 GEMIN6, DHX57, 9 more genes
    nsv6636352copy number variation1nstd102humanUncertain significance GRCh37 chr2: 39,040,762-39,271,911 , GRCh38.p12 chr2: 38,813,620-39,044,770 ARHGEF33, LOC105374470, 7 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6548072inversion1nstd223human GRCh38 chr2: 32,866,995-42,468,982 , GRCh37.p13 chr2: 33,092,062-42,696,122 PKDCC, SRSF7, 127 more genes
    nsv6542757inversion1nstd223human GRCh38 chr2: 32,866,974-42,451,061 , GRCh37.p13 chr2: 33,092,041-42,678,201 RASGRP3, TTC39DP, 125 more genes
    nsv6540167inversion1nstd223human GRCh38 chr2: 32,866,952-40,818,398 , GRCh37.p13 chr2: 33,092,019-41,045,538 CEBPZOS, RNU6-1116P, 110 more genes
    nsv6539485inversion1nstd223human GRCh38 chr2: 32,866,964-42,766,565 , GRCh37.p13 chr2: 33,092,031-42,993,705 RN7SL602P, RNU6-851P, 132 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313619copy number variation1nstd102humanPathogenic GRCh37 chr2: 29,899,368-42,441,440 , GRCh38.p12 chr2: 29,676,502-42,214,300 LOC107985870, SLC25A5P2, 161 more genes
    nsv6262299copy number variation1nstd214human GRCh38 chr2: 38,958,828-38,958,890 , GRCh37.p13 chr2: 39,185,969-39,186,031 ARHGEF33, LOC375196
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6134458copy number variation2nstd213human GRCh37 chr2: 38,440,000-47,670,001 , GRCh38.p12 chr2: 38,212,858-47,442,862 ASS1P2, BCYRN1, 144 more genes
    nsv6134457copy number variation1nstd213human GRCh37 chr2: 38,410,000-75,540,001 , GRCh38.p12 chr2: 38,182,858-75,312,875 , ACTG2, 598 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv4728394copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,012,532-39,548,268 , GRCh38.p12 chr2: 37,785,389-39,321,127 ATL2, LOC375196, 37 more genes
    nsv4452237copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 39,053,852-42,501,893 , GRCh38.p12 chr2: 38,826,710-42,274,753 SLC8A1, SOS1, 38 more genes
    nsv4335876sequence alteration1nstd166human GRCh37.p13 chr2: 20,021,666-53,788,063 , GRCh38.p12 chr2: 19,821,905-53,560,926 , ADCY3, 531 more genes
    nsv4331174inversion1nstd166human GRCh37.p13 chr2: 36,139,982-53,112,348 , GRCh38.p12 chr2: 35,914,916-52,885,210 , ASS1P2, 247 more genes
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