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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142400insertion1nstd232human GRCh37.p13 chr17: 47,007,975-47,007,975 , GRCh38.p12 chr17: 48,930,613-48,930,613 SNF8
    nsv7066099inversion1nstd229human GRCh38 chr17: 48,881,742-49,437,637 , GRCh37.p13 chr17: 46,959,104-47,514,999 B4GALNT2P1, EIF4EP2, 21 more genes
    nsv6984497copy number variation1nstd229human GRCh38 chr17: 48,934,819-48,938,037 , GRCh37.p13 chr17: 47,012,181-47,015,399 SNF8
    nsv6637543copy number variation1nstd102humanUncertain significance GRCh37 chr17: 46,753,824-47,577,721 , GRCh38.p12 chr17: 48,676,462-49,500,359 CALCOCO2, SUMO2P17, 37 more genes
    nsv6591019inversion1nstd223human GRCh38 chr17: 48,939,075-48,939,615 , GRCh37.p13 chr17: 47,016,437-47,016,977 SNF8
    nsv6527146copy number variation1nstd223human GRCh38 chr17: 48,934,818-48,938,036 , GRCh37.p13 chr17: 47,012,180-47,015,398 SNF8
    nsv5970537inversion1nstd209human GRCh38 chr17: 48,889,540-49,449,733 , GRCh37.p13 chr17: 46,966,902-47,527,095 , ATP5MC1, 23 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5298557copy number variation1nstd204human GRCh37.p13 chr17: 46,976,763-47,037,962 , GRCh38.p13 chr17: 48,899,401-48,960,600 GIP, SNF8, 4 more genes
    nsv5013785copy number variation1nstd200human GRCh38 chr17: 48,719,127-49,313,149 , GRCh37.p13 chr17: 46,796,489-47,390,511 , UBE2Z, 30 more genes
    nsv4532435copy number variation1nstd166human GRCh37.p13 chr17: 46,996,581-47,061,042 , GRCh38.p12 chr17: 48,919,219-48,983,680 GIP, SNF8, 2 more genes
    nsv4457643copy number variation1nstd102humanUncertain significance GRCh37 chr17: 46,899,690-47,540,874 , GRCh38.p12 chr17: 48,822,328-49,463,512 FLJ40194, IGF2BP1, 24 more genes
    nsv4457474copy number variation1nstd102humanUncertain significance GRCh37 chr17: 46,874,271-47,158,974 , GRCh38.p12 chr17: 48,796,909-49,081,612 GIP, LOC100419622, 11 more genes
    nsv4338396sequence alteration1nstd166human GRCh37.p13 chr17: 46,959,103-47,527,096 , GRCh38.p12 chr17: 48,881,741-49,449,734 , IGF2BP1, 23 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4270561copy number variation1nstd166human GRCh37.p13 chr17: 47,007,059-47,060,287 , GRCh38.p12 chr17: 48,929,697-48,982,925 GIP, RNU1-42P, 1 more genes
    nsv3920056copy number variation1nstd102humanUncertain significance NCBI36 chr17: 43,882,989-44,985,282 , GRCh38 chr17: 48,450,628-49,552,921 , GRCh37 chr17: 46,527,990-47,630,283 ZNF652-AS1, RPS10P25, 55 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3913486copy number variation1nstd102humanPathogenic GRCh38 chr17: 48,520,885-49,511,208 , NCBI36 chr17: 43,953,246-44,943,569 , GRCh37 chr17: 46,598,247-47,588,570 MIR6165, NGFR, 54 more genes
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