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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096553copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr3: 182,733,226-184,094,097 , GRCh38.p12 chr3: 183,015,438-184,376,309 DVL3, LOC105374247, 51 more genes
    nsv7044730inversion1nstd229human GRCh38 chr3: 183,134,725-183,134,847 , GRCh37.p13 chr3: 182,852,513-182,852,635 LAMP3
    nsv6734439copy number variation1nstd229human GRCh38 chr3: 183,134,673-183,205,635 , GRCh37.p13 chr3: 182,852,461-182,923,423 SNORD3P4, MCF2L2, 1 more genes
    nsv6730885copy number variation1nstd229human GRCh38 chr3: 183,137,201-183,156,100 , GRCh37.p13 chr3: 182,854,989-182,873,888 LAMP3
    nsv6728983copy number variation1nstd229human GRCh38 chr3: 183,084,601-183,121,800 , GRCh37.p13 chr3: 182,802,389-182,839,588 MCCC1, LOC105374247, 1 more genes
    nsv6725815copy number variation1nstd229human GRCh38 chr3: 183,152,594-183,176,156 , GRCh37.p13 chr3: 182,870,382-182,893,944 MCF2L2, SNORD3P4, 1 more genes
    nsv6723673copy number variation1nstd229human GRCh38 chr3: 183,124,551-183,134,710 , GRCh37.p13 chr3: 182,842,339-182,852,498 LAMP3
    nsv6634384copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,062,175-185,474,509 , GRCh38.p12 chr3: 181,344,387-185,756,721 PRICKLE1P1, KLHL24, 99 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6373820copy number variation1nstd223human GRCh38 chr3: 183,138,032-183,142,066 , GRCh37.p13 chr3: 182,855,820-182,859,854 LAMP3
    nsv6372725copy number variation1nstd223human GRCh38 chr3: 183,137,101-183,138,800 , GRCh37.p13 chr3: 182,854,889-182,856,588 LAMP3
    nsv6360633copy number variation1nstd223human GRCh38 chr3: 183,145,697-183,156,108 , GRCh37.p13 chr3: 182,863,485-182,873,896 LAMP3
    nsv6313539copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,189,525-187,212,935 , GRCh38.p12 chr3: 182,471,737-187,495,147 ALG3, MIR4448, 133 more genes
    nsv6290246copy number variation1nstd102humanPathogenic GRCh37 chr3: 175,119,199-187,592,480 , GRCh38.p12 chr3: 175,401,410-187,874,692 RPL39L, MCF2L2, 220 more genes
    nsv6135005copy number variation1nstd213human GRCh37 chr3: 182,560,000-183,260,001 , GRCh38.p12 chr3: 182,842,212-183,542,213 SNORD3P4, KLHL6, 15 more genes
    nsv5948512insertion1nstd209human GRCh38 chr3: 183,149,575-183,149,575 , GRCh37.p13 chr3: 182,867,363-182,867,363 LAMP3
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5451852copy number variation1nstd206human GRCh38 chr3: 183,134,673-183,205,635 , GRCh37.p13 chr3: 182,852,461-182,923,423 SNORD3P4, LAMP3, 1 more genes
    nsv4805048copy number variation1nstd200human GRCh37 chr3: 182,880,789-182,885,188 , GRCh38.p12 chr3: 183,163,001-183,167,400 LAMP3
    nsv4805047copy number variation1nstd200human GRCh37 chr3: 182,863,442-182,864,991 , GRCh38.p12 chr3: 183,145,654-183,147,203 LAMP3
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