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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096704copy number variation1nstd102humanUncertain significance GRCh37 chr3: 168,802,697-172,835,521 , GRCh38.p12 chr3: 169,084,909-173,117,731 GHSR, KLF7P1, 67 more genes
    nsv7057325inversion1nstd229human GRCh38 chr3: 170,134,629-173,143,661 , GRCh37.p13 chr3: 169,852,417-172,861,451 LINC02068, LOC107986052, 45 more genes
    nsv7050298inversion1nstd229human GRCh38 chr3: 172,648,347-172,652,220 , GRCh37.p13 chr3: 172,366,137-172,370,010 NCEH1
    nsv6736048copy number variation1nstd229human GRCh38 chr3: 172,640,032-172,645,448 , GRCh37.p13 chr3: 172,357,822-172,363,238 NCEH1
    nsv6732591copy number variation1nstd229human GRCh38 chr3: 172,612,012-172,681,673 , GRCh37.p13 chr3: 172,329,802-172,399,463 NCEH1, NAP1L5P1
    nsv6729904copy number variation1nstd229human GRCh38 chr3: 172,683,122-172,683,430 , GRCh37.p13 chr3: 172,400,912-172,401,220 NCEH1
    nsv6724070copy number variation1nstd229human GRCh38 chr3: 172,647,701-172,665,345 , GRCh37.p13 chr3: 172,365,491-172,383,135 NCEH1
    nsv6723959copy number variation1nstd229human GRCh38 chr3: 172,640,901-172,643,400 , GRCh37.p13 chr3: 172,358,691-172,361,190 NCEH1
    nsv6722139copy number variation1nstd229human GRCh38 chr3: 172,612,562-172,698,050 , GRCh37.p13 chr3: 172,330,352-172,415,840 NCEH1, NAP1L5P1
    nsv6721206copy number variation1nstd229human GRCh38 chr3: 172,672,998-172,759,318 , GRCh37.p13 chr3: 172,390,788-172,477,108 RNU6-547P, NCEH1, 2 more genes
    nsv6720355copy number variation1nstd229human GRCh38 chr3: 172,711,020-172,721,727 , GRCh37.p13 chr3: 172,428,810-172,439,517 NCEH1
    nsv6720221copy number variation1nstd229human GRCh38 chr3: 172,646,335-172,653,558 , GRCh37.p13 chr3: 172,364,125-172,371,348 NCEH1
    nsv6636531copy number variation1nstd102humanUncertain significance GRCh37 chr3: 172,266,023-172,500,533 , GRCh38.p12 chr3: 172,548,233-172,782,743 LINC02068, RNU6-547P, 4 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
    nsv6569947inversion1nstd223human GRCh38 chr3: 172,650,409-172,651,857 , GRCh37.p13 chr3: 172,368,199-172,369,647 NCEH1
    nsv6558545inversion1nstd223human GRCh38 chr3: 172,705,734-172,706,579 , GRCh37.p13 chr3: 172,423,524-172,424,369 NCEH1
    nsv6556602inversion1nstd223human GRCh38 chr3: 172,688,136-172,689,364 , GRCh37.p13 chr3: 172,405,926-172,407,154 NCEH1
    nsv6368889copy number variation1nstd223human GRCh38 chr3: 172,634,066-172,636,543 , GRCh37.p13 chr3: 172,351,856-172,354,333 NCEH1
    nsv6367074copy number variation1nstd223human GRCh38 chr3: 172,683,122-172,683,430 , GRCh37.p13 chr3: 172,400,912-172,401,220 NCEH1
    nsv6365053copy number variation1nstd223human GRCh38 chr3: 172,702,713-172,704,734 , GRCh37.p13 chr3: 172,420,503-172,422,524 NCEH1, RNU6-547P
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