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 300

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148088copy number variation1nstd102humanUncertain significance GRCh37 chr17: 25,263,507-27,829,791 , GRCh38.p12 chr17: 26,936,481-29,502,773 RNU4-34P, RNU6-711P, 95 more genes
    nsv7095084copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155 RNU6-1267P, PIPOX, 114 more genes
    nsv7094962copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-27,581,367 , GRCh38.p12 chr17: 28,357,671-29,254,349 FLOT2, SPAG5-AS1, 50 more genes
    nsv7069498inversion1nstd229human GRCh38 chr17: 29,125,325-29,125,458 , GRCh37.p13 chr17: 27,452,343-27,452,476 MYO18A
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv6997353copy number variation1nstd229human GRCh38 chr17: 29,105,064-29,191,372 , GRCh37.p13 chr17: 27,432,082-27,518,390 MYO18A
    nsv6997211copy number variation1nstd229human GRCh38 chr17: 29,141,976-29,144,983 , GRCh37.p13 chr17: 27,468,994-27,472,001 MYO18A
    nsv6995825copy number variation1nstd229human GRCh38 chr17: 29,072,659-29,074,856 , GRCh37.p13 chr17: 27,399,677-27,401,874 MYO18A
    nsv6995455copy number variation1nstd229human GRCh38 chr17: 29,132,797-29,133,041 , GRCh37.p13 chr17: 27,459,815-27,460,059 MYO18A
    nsv6993461copy number variation1nstd229human GRCh38 chr17: 29,160,561-29,164,412 , GRCh37.p13 chr17: 27,487,579-27,491,430 MYO18A
    nsv6989120copy number variation1nstd229human GRCh38 chr17: 29,130,501-29,140,821 , GRCh37.p13 chr17: 27,457,519-27,467,839 MYO18A
    nsv6987181copy number variation1nstd229human GRCh38 chr17: 29,140,791-29,144,097 , GRCh37.p13 chr17: 27,467,809-27,471,115 MYO18A
    nsv6983267copy number variation1nstd229human GRCh38 chr17: 29,168,438-29,168,495 , GRCh37.p13 chr17: 27,495,456-27,495,513 MYO18A
    nsv6981313copy number variation1nstd229human GRCh38 chr17: 29,087,743-29,088,354 , GRCh37.p13 chr17: 27,414,761-27,415,372 MYO18A
    nsv6980451copy number variation1nstd229human GRCh38 chr17: 29,103,792-32,176,512 , GRCh37.p13 chr17: 27,430,810-30,503,531 SMURF2P1-LRRC37BP1, RNU6-990P, 90 more genes
    nsv6979578copy number variation1nstd229human GRCh38 chr17: 29,050,201-29,069,800 , GRCh37.p13 chr17: 27,377,219-27,396,818 PIPOX, MYO18A
    nsv6576729inversion1nstd223human GRCh38 chr17: 29,096,547-29,097,169 , GRCh37.p13 chr17: 27,423,565-27,424,187 MYO18A
    nsv6514121copy number variation1nstd223human GRCh38 chr17: 29,139,909-29,143,709 , GRCh37.p13 chr17: 27,466,927-27,470,727 MYO18A
    nsv6512957copy number variation1nstd223human GRCh38 chr17: 29,105,796-29,106,061 , GRCh37.p13 chr17: 27,432,814-27,433,079 MYO18A
    nsv6511939copy number variation1nstd223human GRCh38 chr17: 29,130,501-29,140,801 , GRCh37.p13 chr17: 27,457,519-27,467,819 MYO18A
    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