U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 415

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095334copy number variation2nstd102humanUncertain significance GRCh37 chr17: 40,376,777-40,575,115 , GRCh38.p12 chr17: 42,224,759-42,423,097 STAT5A, CAVIN1, 3 more genes
    nsv7095153copy number variation1nstd102humanUncertain significance GRCh37 chr17: 40,467,763-40,467,838 , GRCh38.p12 chr17: 42,315,745-42,315,820 STAT3
    nsv7094886copy number variation1nstd102humanUncertain significance GRCh37 chr17: 40,481,408-40,491,447 , GRCh38.p12 chr17: 42,329,390-42,339,429 STAT3
    nsv6995985copy number variation1nstd229human GRCh38 chr17: 42,359,799-42,359,844 , GRCh37.p13 chr17: 40,511,817-40,511,862 STAT3
    nsv6995364copy number variation1nstd229human GRCh38 chr17: 42,335,428-42,335,645 , GRCh37.p13 chr17: 40,487,446-40,487,663 STAT3
    nsv6995227copy number variation1nstd229human GRCh38 chr17: 42,327,302-42,328,096 , GRCh37.p13 chr17: 40,479,320-40,480,114 STAT3
    nsv6990543copy number variation1nstd229human GRCh38 chr17: 42,376,039-42,379,958 , GRCh37.p13 chr17: 40,528,057-40,531,976 STAT3
    nsv6985374copy number variation1nstd229human GRCh38 chr17: 42,342,504-42,342,971 , GRCh37.p13 chr17: 40,494,522-40,494,989 STAT3
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6983489copy number variation1nstd229human GRCh38 chr17: 42,361,501-42,362,800 , GRCh37.p13 chr17: 40,513,519-40,514,818 STAT3
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6593339inversion1nstd223human GRCh38 chr17: 42,328,004-42,328,549 , GRCh37.p13 chr17: 40,480,022-40,480,567 STAT3
    nsv6590104inversion1nstd223human GRCh38 chr17: 42,320,635-42,321,381 , GRCh37.p13 chr17: 40,472,653-40,473,399 STAT3
    nsv6588436inversion1nstd223human GRCh38 chr17: 42,330,462-42,332,552 , GRCh37.p13 chr17: 40,482,480-40,484,570 STAT3
    nsv6582839inversion1nstd223human GRCh38 chr17: 42,330,139-42,332,845 , GRCh37.p13 chr17: 40,482,157-40,484,863 STAT3
    nsv6582731inversion1nstd223human GRCh38 chr17: 42,332,072-42,332,460 , GRCh37.p13 chr17: 40,484,090-40,484,478 STAT3
    nsv6582391inversion1nstd223human GRCh38 chr17: 42,318,149-42,319,061 , GRCh37.p13 chr17: 40,470,167-40,471,079 STAT3
    nsv6579923inversion1nstd223human GRCh38 chr17: 42,384,133-42,385,524 , GRCh37.p13 chr17: 40,536,151-40,537,542 STAT3
    nsv6513387copy number variation1nstd223human GRCh38 chr17: 42,353,291-42,374,516 , GRCh37.p13 chr17: 40,505,309-40,526,534 STAT3
    nsv6513020copy number variation1nstd223human GRCh38 chr17: 42,352,142-42,354,685 , GRCh37.p13 chr17: 40,504,160-40,506,703 STAT3
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center