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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6691669copy number variation1nstd229human GRCh38 chr2: 87,425,578-90,288,757 , GRCh37.p13 chr2: 87,652,701-90,295,274 LOC105374854, IGKV1-22, 130 more genes
    nsv6690077copy number variation1nstd229human GRCh38 chr2: 87,635,263-87,662,856 , GRCh37.p13 chr2: 87,934,782-87,962,375 LOC101928214, RPS14P5
    nsv6634812copy number variation1nstd227human GRCh37 chr2: 87,430,727-87,965,359 , GRCh38.p12 chr2: 87,203,604-87,665,840 PAFAH1B1P1, CYTOR, 13 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
    nsv6628421copy number variation1nstd224human GRCh37 chr2: 87,479,689-87,974,847 , GRCh38.p12 chr2: 87,252,566-87,675,328 RPS14P5, LOC105377635, 11 more genes
    nsv6628420copy number variation1nstd224human GRCh37 chr2: 87,479,689-87,965,359 , GRCh38.p12 chr2: 87,252,566-87,665,840 CYTOR, MIR4435-1, 11 more genes
    nsv6628417copy number variation3nstd224human GRCh37 chr2: 87,394,756-87,965,359 , GRCh38.p12 chr2: 87,167,633-87,665,840 CYTOR, CENPNP1, 14 more genes
    nsv6628360copy number variation6nstd224human GRCh37 chr2: 87,405,001-88,215,335 , GRCh38.p12 chr2: 87,177,878-87,915,816 PLGLB2, PAFAH1B1P1, 19 more genes
    nsv6628359copy number variation1nstd224human GRCh37 chr2: 87,395,619-87,965,359 , GRCh38.p12 chr2: 87,168,496-87,665,840 MIR4771-1, LOC101928214, 14 more genes
    nsv6628228copy number variation2nstd224human GRCh37 chr2: 87,394,756-88,045,046 , GRCh38.p12 chr2: 87,167,633-87,745,527 PAFAH1B1P1, ANAPC1P4, 15 more genes
    nsv6628227copy number variation4nstd224human GRCh37 chr2: 87,394,756-87,974,847 , GRCh38.p12 chr2: 87,167,633-87,675,328 CENPNP1, LOC105374848, 14 more genes
    nsv6628164copy number variation1nstd224human GRCh37 chr2: 87,479,689-88,045,046 , GRCh38.p12 chr2: 87,252,566-87,745,527 LINC01955, LOC107985909, 12 more genes
    nsv6628163copy number variation19nstd224human GRCh37 chr2: 87,405,001-87,965,359 , GRCh38.p12 chr2: 87,177,878-87,665,840 CENPNP1, LOC101928214, 14 more genes
    nsv6553936inversion1nstd223human GRCh38 chr2: 86,913,704-87,825,694 , GRCh37.p13 chr2: 87,140,827-88,125,213 ANAPC1P2, CYTOR, 27 more genes
    nsv6547455inversion1nstd223human GRCh38 chr2: 86,913,968-87,825,588 , GRCh37.p13 chr2: 87,141,091-88,125,107 DBF4P3, LOC102724642, 27 more genes
    nsv6339167copy number variation1nstd223human GRCh38 chr2: 87,147,106-87,722,815 , GRCh37.p13 chr2: 87,374,229-88,022,334 ANAPC1P4, LOC105374848, 16 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv5990588copy number variation1nstd212human GRCh38 chr2: 87,653,660-87,653,717 , GRCh37.p13 chr2: 87,953,179-87,953,236 RPS14P5
    nsv5670092inversion1nstd207human GRCh38 chr2: 87,362,763-87,699,046 , GRCh37.p13 chr2: 87,589,886-87,998,565 , PAFAH1B1P1, 7 more genes
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