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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv5902204copy number variation1nstd209human GRCh38 chr3: 136,844,541-136,846,902 , GRCh37.p13 chr3: 136,563,383-136,565,744 NCK1-DT, SLC35G2
    nsv5834674copy number variation1nstd209human GRCh38 chr3: 136,844,861-136,846,777 , GRCh37.p13 chr3: 136,563,703-136,565,619 SLC35G2, NCK1-DT
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4927963copy number variation1nstd200human GRCh38 chr3: 136,860,216-136,861,613 , GRCh37.p13 chr3: 136,579,058-136,580,455 NCK1, NCK1-DT
    nsv4927962copy number variation1nstd200human GRCh38 chr3: 136,847,509-136,847,789 , GRCh37.p13 chr3: 136,566,351-136,566,631 NCK1-DT, SLC35G2
    nsv4927961copy number variation1nstd200human GRCh38 chr3: 136,844,556-136,846,889 , GRCh37.p13 chr3: 136,563,398-136,565,731 SLC35G2, NCK1-DT
    nsv4927960copy number variation1nstd200human GRCh38 chr3: 136,843,118-136,851,336 , GRCh37.p13 chr3: 136,561,960-136,570,178 SLC35G2, NCK1-DT
    nsv4791186copy number variation1nstd200human GRCh37 chr3: 136,566,351-136,566,631 , GRCh38.p12 chr3: 136,847,509-136,847,789 NCK1-DT, SLC35G2
    nsv4791185copy number variation1nstd200human GRCh37 chr3: 136,563,398-136,565,732 , GRCh38.p12 chr3: 136,844,556-136,846,890 NCK1-DT, SLC35G2
    nsv4791184copy number variation1nstd200human GRCh37 chr3: 136,561,938-136,562,515 , GRCh38.p12 chr3: 136,843,096-136,843,673 SLC35G2, NCK1-DT
    nsv4451778copy number variation1nstd102humanUncertain significance GRCh37 chr3: 135,186,881-140,826,836 , GRCh38.p12 chr3: 135,468,039-141,107,994 ARMC8, EEF1A1P25, 73 more genes
    nsv4387003copy number variation1nstd173human GRCh37 chr3: 136,580,487-136,604,563 , GRCh38.p12 chr3: 136,861,645-136,885,721 NCK1, NCK1-DT
    nsv4369181copy number variation2nstd173human GRCh37 chr3: 136,580,487-136,604,382 , GRCh38.p12 chr3: 136,861,645-136,885,540 NCK1, NCK1-DT
    nsv4347615copy number variation1nstd102humanPathogenic GRCh37 chr3: 135,288,025-146,874,012 , GRCh38.p12 chr3: 135,569,183-147,156,225 RPL6P9, NME9, 145 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv4112249copy number variation1nstd166human GRCh37.p13 chr3: 136,562,047-136,570,210 , GRCh38.p12 chr3: 136,843,205-136,851,368 SLC35G2, NCK1-DT
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3921636copy number variation1nstd102humanPathogenic GRCh38 chr3: 135,227,451-145,870,770 , NCBI36 chr3: 136,428,983-147,071,247 , GRCh37 chr3: 134,946,293-145,588,557 A4GNT, TRIM42, 134 more genes
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