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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048533inversion1nstd229human GRCh38 chr3: 161,386,305-161,956,957 , GRCh37.p13 chr3: 161,104,093-161,674,745 RPL23AP42, LINC02067, 2 more genes
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv6731372copy number variation1nstd229human GRCh38 chr3: 161,438,909-161,438,946 , GRCh37.p13 chr3: 161,156,697-161,156,734 LINC02067
    nsv6722497copy number variation1nstd229human GRCh38 chr3: 161,334,993-162,113,025 , GRCh37.p13 chr3: 161,052,781-161,830,813 OTOL1, LINC02067, 3 more genes
    nsv6720541copy number variation1nstd229human GRCh38 chr3: 160,927,633-161,461,576 , GRCh37.p13 chr3: 160,645,421-161,179,364 LOC112268450, PPM1L, 10 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6562725inversion1nstd223human GRCh38 chr3: 161,386,305-161,956,957 , GRCh37.p13 chr3: 161,104,093-161,674,745 OTOL1, RPL23AP42, 2 more genes
    nsv6362931copy number variation1nstd223human GRCh38 chr3: 161,334,993-162,113,020 , GRCh37.p13 chr3: 161,052,781-161,830,808 LINC02067, SPTSSB, 3 more genes
    nsv6359997copy number variation1nstd223human GRCh38 chr3: 161,445,582-161,446,216 , GRCh37.p13 chr3: 161,163,370-161,164,004 LINC02067
    nsv6291134copy number variation1nstd102humanLikely benign GRCh37 chr3: 160,826,404-161,251,252 , GRCh38.p12 chr3: 161,108,616-161,533,464 LOC105374186, PSMC1P7, 9 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6209800insertion1nstd214human GRCh38 chr3: 161,438,914-161,438,914 , GRCh37.p13 chr3: 161,156,702-161,156,702 LINC02067
    nsv6134788copy number variation1nstd213human GRCh37 chr3: 155,010,000-169,630,001 , GRCh38.p12 chr3: 155,292,211-169,912,213 , BCHE, 171 more genes
    nsv6063371insertion1nstd212human GRCh38 chr3: 161,438,914-161,438,914 , GRCh37.p13 chr3: 161,156,702-161,156,702 LINC02067
    nsv5949619insertion1nstd209human GRCh38 chr3: 161,438,914-161,438,914 , GRCh37.p13 chr3: 161,156,702-161,156,702 LINC02067
    nsv5692601mobile element insertion1nstd211human GRCh38 chr3: 161,425,965-161,425,965 , GRCh37.p13 chr3: 161,143,753-161,143,753 LINC02067
    nsv5606764insertion1nstd207human GRCh38 chr3: 161,438,914-161,438,914 , GRCh37.p13 chr3: 161,156,702-161,156,702 LINC02067
    nsv5560984sequence alteration1nstd206human GRCh37.p13 chr3: 161,086,425-162,243,749 , GRCh38 chr3: 161,368,637-162,525,961 OTOL1, SPTSSB, 6 more genes
    nsv5538574insertion1nstd206human GRCh38 chr3: 161,438,946-161,438,965 , GRCh37.p13 chr3: 161,156,734-161,156,753 LINC02067
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
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