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 75

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094423copy number variation2nstd102humanUncertain significance GRCh37 chr14: 23,242,819-25,103,366 , GRCh38.p12 chr14: 22,773,610-24,634,160 LINC00596, NGDN, 107 more genes
    nsv7074310inversion1nstd229human GRCh38 chr14: 22,076,285-27,854,954 , GRCh37.p13 chr14: 22,544,546-28,324,160 PPP1R3E, TRAJ37, 242 more genes
    nsv7070619inversion1nstd229human GRCh38 chr14: 23,713,943-24,501,695 , GRCh37.p13 chr14: 24,183,152-24,970,901 TSSK4, RIPK3, 48 more genes
    nsv6946215copy number variation1nstd229human GRCh38 chr14: 24,192,852-24,193,217 , GRCh37.p13 chr14: 24,662,058-24,662,423 TM9SF1
    nsv6941402copy number variation1nstd229human GRCh38 chr14: 24,059,301-24,305,100 , GRCh37.p13 chr14: 24,528,510-24,774,306 PSME2, CIDEB, 27 more genes
    nsv6480499copy number variation1nstd223human GRCh38 chr14: 24,193,675-24,200,205 , GRCh37.p13 chr14: 24,662,881-24,669,411 TM9SF1
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv6132776copy number variation1nstd213human GRCh37 chr14: 24,490,000-28,000,001 , GRCh38.p12 chr14: 24,020,791-27,530,795 CMA1, LTB4R, 65 more genes
    nsv6036569copy number variation1nstd212human GRCh38 chr14: 24,193,768-24,193,843 , GRCh37.p13 chr14: 24,662,974-24,663,049 TM9SF1
    nsv6034094copy number variation1nstd212human GRCh38 chr14: 24,193,474-24,193,553 , GRCh37.p13 chr14: 24,662,680-24,662,759 TM9SF1
    nsv5263479copy number variation1nstd204human GRCh38.p13 chr14: 24,019,501-24,275,100 , GRCh37.p13 chr14: 24,488,710-24,744,306 , RABGGTA, 26 more genes
    nsv4728842copy number variation1nstd102humanUncertain significance GRCh37 chr14: 24,163,771-24,818,728 , GRCh38.p12 chr14: 23,694,562-24,347,428 , GRCh38.p12 chr14|NW_018654722.1: 1-650,500 FITM1, CIDEB, 44 more genes
    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
    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
    nsv4349901copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,100,682-28,730,087 , GRCh38.p12 chr14: 18,324,205-28,260,881 TRAV4, UNGP2, 458 more genes
    nsv3922265copy number variation1nstd102humanLikely pathogenic NCBI36 chr14: 19,950,586-24,557,166 , GRCh37 chr14: 20,880,746-25,487,326 , GRCh38 chr14: 20,412,587-25,018,120 ANG, APEX1, 346 more genes
    nsv3919655copy number variation1nstd102humanPathogenic GRCh37 chr14: 24,453,274-25,843,700 , GRCh38 chr14: 23,984,065-25,374,494 , NCBI36 chr14: 23,523,114-24,913,540 NFATC4, LTB4R, 50 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3918965copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,490,852-44,562,875 , GRCh38 chr14: 20,022,693-44,093,672 , NCBI36 chr14: 19,560,692-43,632,625 TRAJ13, LRP10, 589 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