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 125

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7072074inversion1nstd229human GRCh38 chr17: 10,322,193-11,492,057 , GRCh37.p13 chr17: 10,225,510-11,395,374 ADPRM, MYH4, 18 more genes
    nsv6997035copy number variation1nstd229human GRCh38 chr17: 9,981,556-11,548,056 , GRCh37.p13 chr17: 9,884,873-11,451,373 LOC107985004, MYH2, 20 more genes
    nsv6993743copy number variation1nstd229human GRCh38 chr17: 10,658,774-11,321,014 , GRCh37.p13 chr17: 10,562,091-11,224,331 MYH3, SCO1, 11 more genes
    nsv6993504copy number variation1nstd229human GRCh38 chr17: 10,690,924-10,747,710 , GRCh37.p13 chr17: 10,594,241-10,651,027 ADPRM, TMEM220, 3 more genes
    nsv6989889copy number variation1nstd229human GRCh38 chr17: 10,314,520-10,737,161 , GRCh37.p13 chr17: 10,217,837-10,640,478 MYH3, MAGOH2P, 11 more genes
    nsv6989092copy number variation1nstd229human GRCh38 chr17: 10,322,350-10,944,267 , GRCh37.p13 chr17: 10,225,667-10,847,584 LOC105371536, MYH4, 16 more genes
    nsv6987986copy number variation1nstd229human GRCh38 chr17: 10,184,262-10,772,232 , GRCh37.p13 chr17: 10,087,579-10,675,549 MYH2, MYH8, 13 more genes
    nsv6638024copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,517,286-10,814,075 , GRCh38.p12 chr17: 10,613,969-10,910,758 SCO1, TMEM220-AS1, 10 more genes
    nsv6506694copy number variation1nstd223human GRCh38 chr17: 10,615,797-10,787,245 , GRCh37.p13 chr17: 10,519,114-10,690,562 MYH3, TMEM220-AS1, 5 more genes
    nsv6133324copy number variation1nstd213human GRCh37 chr17: 9,930,000-12,980,001 , GRCh38.p12 chr17: 10,026,683-13,076,684 DNAH9, MYH1, 36 more genes
    nsv6133292copy number variation1nstd213human GRCh37 chr17: 10,450,000-10,630,001 , GRCh38.p12 chr17: 10,546,683-10,726,684 MYH2, MYH3, 5 more genes
    nsv5929452copy number variation1nstd209human GRCh38 chr17: 6,412,133-13,962,466 , GRCh37.p13 chr17: 6,315,453-13,865,783 , PIK3R5-DT, 226 more genes
    nsv5530125copy number variation1nstd206human GRCh38 chr17: 10,710,688-10,748,136 , GRCh37.p13 chr17: 10,614,005-10,651,453 TMEM220-AS1, MAGOH2P, 2 more genes
    nsv5023666copy number variation1nstd200human GRCh38 chr17: 10,615,797-10,787,245 , GRCh37.p13 chr17: 10,519,114-10,690,562 SCO1, ADPRM, 5 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4684245copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,493,837-15,099,023 , GRCh38.p12 chr17: 10,590,520-15,195,706 LOC100506974, MIR1269B, 52 more genes
    nsv4628981copy number variation1nstd183human GRCh37 chr17: 10,613,996-10,651,448 , GRCh38.p12 chr17: 10,710,679-10,748,131 ADPRM, TMEM220, 2 more genes
    nsv4457480copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,604,119-10,744,366 , GRCh38.p12 chr17: 10,700,802-10,841,049 ADPRM, TMEM220, 4 more genes
    nsv4436354complex substitution1nstd102humanUncertain significance GRCh37 chr17: 9,586,165-16,325,968 , GRCh38.p12 chr17: 9,682,848-16,422,654 ADORA2B, COX10, 109 more genes
    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