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 202

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938665copy number variation1nstd209human GRCh38 chr14: 21,067,972-21,068,297 , GRCh37.p13 chr14: 21,536,131-21,536,456 NDRG2, ARHGEF40
    nsv5594522copy number variation1nstd207human GRCh38 chr14: 21,067,972-21,068,297 , GRCh37.p13 chr14: 21,536,131-21,536,456 NDRG2, ARHGEF40
    nsv5512724copy number variation1nstd206human GRCh38 chr14: 21,063,773-21,064,083 , GRCh37.p13 chr14: 21,531,932-21,532,242 ARHGEF40, NDRG2
    nsv5494696copy number variation1nstd206human GRCh38 chr14: 21,067,985-21,068,298 , GRCh37.p13 chr14: 21,536,144-21,536,457 NDRG2, ARHGEF40
    nsv5385185mobile element deletion2nstd186human GRCh37 chr14: 21,536,144-21,536,457 , GRCh38.p12 chr14: 21,067,985-21,068,298 NDRG2, ARHGEF40
    nsv5203420mobile element deletion1nstd204human GRCh37.p13 chr14: 21,536,144-21,536,457 , GRCh38.p13 chr14: 21,067,985-21,068,298 ARHGEF40, NDRG2
    nsv4899963mobile element deletion1nstd200human GRCh38 chr14: 21,067,985-21,068,298 , GRCh37.p13 chr14: 21,536,144-21,536,457 ARHGEF40, NDRG2
    nsv4775328mobile element deletion1nstd200human GRCh37 chr14: 21,536,144-21,536,457 , GRCh38.p12 chr14: 21,067,985-21,068,298 NDRG2, ARHGEF40
    nsv4746242copy number variation1nstd199human GRCh37 chr14: 21,536,132-21,536,459 , GRCh38.p12 chr14: 21,067,973-21,068,300 NDRG2, ARHGEF40
    nsv4729394copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-21,915,516 , GRCh38.p12 chr14: 20,043,513-21,447,357 SETP1, OR11H5P, 99 more genes
    nsv4711862copy number variation2nstd195human GRCh37 chr14: 21,536,131-21,536,132 , GRCh38.p12 chr14: 21,067,972-21,067,973 ARHGEF40, NDRG2
    nsv4685750copy number variation1nstd102humannot provided GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685 IGBP1P1, RAB2B, 579 more genes
    nsv4676085copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,143,933-23,297,667 , GRCh38.p12 chr14: 20,675,774-22,828,458 ANG, SNORD8, 209 more genes
    nsv4675977copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 21,159,605-22,252,320 , GRCh38.p12 chr14: 20,691,446-21,784,103 ANG, HNRNPC, 69 more genes
    nsv4675943copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827 TRAJ36, SEC23A-AS1, 590 more genes
    nsv4673211copy number variation1nstd186human GRCh37 chr14: 21,544,812-21,544,858 , GRCh38.p12 chr14: 21,076,653-21,076,699 ARHGEF40
    nsv4655237copy number variation2nstd186human GRCh37 chr14: 21,536,144-21,536,457 , GRCh38.p12 chr14: 21,067,985-21,068,298 ARHGEF40, NDRG2
    nsv4635968mobile element deletion1nstd186human GRCh37 chr14: 21,536,132-21,536,457 , GRCh38.p12 chr14: 21,067,973-21,068,298 ARHGEF40, NDRG2
    nsv4630948copy number variation1nstd183human GRCh37 chr14: 21,544,812-21,544,966 , GRCh38.p12 chr14: 21,076,653-21,076,807 ARHGEF40
    nsv4629644copy number variation1nstd183human GRCh37 chr14: 21,496,021-21,671,277 , GRCh38.p12 chr14: 21,027,862-21,203,118 RNASE13, RNU6-252P, 15 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