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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076079inversion1nstd229human GRCh38 chr16: 9,015,595-14,846,246 , GRCh37.p13 chr16: 9,109,452-14,940,103 LOC105371093, RNU6-633P, 100 more genes
    nsv6966660copy number variation1nstd229human GRCh38 chr16: 14,314,901-14,332,600 , GRCh37.p13 chr16: 14,408,758-14,426,457 MIR193BHG
    nsv6965574copy number variation1nstd229human GRCh38 chr16: 14,268,501-14,452,500 , GRCh37.p13 chr16: 14,362,358-14,546,357 PARN, MIR193B, 4 more genes
    nsv6964397copy number variation1nstd229human GRCh38 chr16: 14,324,281-14,392,453 , GRCh37.p13 chr16: 14,418,138-14,486,310 LINC02130, MIR193BHG
    nsv6962665copy number variation1nstd229human GRCh38 chr16: 14,287,569-14,300,924 , GRCh37.p13 chr16: 14,381,426-14,394,781 MIR193BHG
    nsv6962608copy number variation1nstd229human GRCh38 chr16: 14,314,960-14,319,532 , GRCh37.p13 chr16: 14,408,817-14,413,389 MIR193BHG
    nsv6961268copy number variation1nstd229human GRCh38 chr16: 14,274,401-14,452,100 , GRCh37.p13 chr16: 14,368,258-14,545,957 TRT-CGT2-1, MIR193BHG, 4 more genes
    nsv6960392copy number variation1nstd229human GRCh38 chr16: 14,314,801-14,321,400 , GRCh37.p13 chr16: 14,408,658-14,415,257 MIR193BHG
    nsv6959603copy number variation1nstd229human GRCh38 chr16: 14,318,065-14,369,123 , GRCh37.p13 chr16: 14,411,922-14,462,980 MIR193BHG, LINC02130
    nsv6637442copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,365,745-17,052,798 , GRCh38.p12 chr16: 14,271,888-16,958,941 ABCC6, ABCC1, 69 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6513973copy number variation1nstd223human GRCh38 chr16: 14,324,281-14,392,425 , GRCh37.p13 chr16: 14,418,138-14,486,282 LINC02130, MIR193BHG
    nsv6501877copy number variation1nstd223human GRCh38 chr16: 14,286,497-14,309,905 , GRCh37.p13 chr16: 14,380,354-14,403,762 MIR193BHG, MIR365A, 1 more genes
    nsv6498926copy number variation1nstd223human GRCh38 chr16: 14,317,278-14,321,213 , GRCh37.p13 chr16: 14,411,135-14,415,070 MIR193BHG
    nsv6309988copy number variation1nstd102humanUncertain significance GRCh37 chr16: 13,915,808-14,724,045 , GRCh38.p12 chr16: 13,821,951-14,630,188 TRT-CGT2-1, RN7SL274P, 14 more genes
    nsv6190251copy number variation1nstd214human GRCh38 chr16: 14,316,031-14,316,127 , GRCh37.p13 chr16: 14,409,888-14,409,984 MIR193BHG
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6133257copy number variation1nstd213human GRCh37 chr16: 14,270,000-14,900,001 , GRCh38.p12 chr16: 14,176,143-14,806,144 , GRCh38.p12 chr16|NT_187607.1: 1-565,201 , PARN, 25 more genes
    nsv6133178copy number variation1nstd213human GRCh37 chr16: 13,470,000-14,990,001 , GRCh38.p12 chr16: 13,376,143-14,896,144 , ERCC4, 26 more genes
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
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