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 85

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5515372copy number variation1nstd206human GRCh38 chr19: 46,607,186-46,607,252 , GRCh37.p13 chr19: 47,110,443-47,110,509 CALM3
    nsv4682791copy number variation1nstd102humanUncertain significance GRCh37 chr19: 47,109,074-47,260,205 , GRCh38.p12 chr19: 46,605,817-46,756,948 DACT3, FKRP, 9 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676350copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920 NKPD1, IGFL1, 112 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4350827copy number variation1nstd102humanPathogenic GRCh37 chr19: 47,036,361-48,525,536 , GRCh38.p12 chr19: 46,533,104-48,022,279 LINC01595, SNAR-A13, 59 more genes
    nsv4321864inversion1nstd166human GRCh37.p13 chr19: 46,657,897-51,634,775 , GRCh38.p12 chr19: 46,154,640-51,131,518 , C5AR1, 288 more genes
    nsv3956484insertion1nstd168human GRCh38 chr19: 46,602,113-46,610,877 , GRCh37.p13 chr19: 47,105,370-47,114,134 CALM3, PTGIR
    nsv3924836copy number variation1nstd102humanPathogenic NCBI36 chr19: 50,166,517-53,452,471 , GRCh37 chr19: 45,474,677-48,760,659 , GRCh38 chr19: 44,971,420-48,257,402 IGFL1P1, LOC105372426, 145 more genes
    nsv3921787copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 50,582,487-52,026,097 , GRCh37 chr19: 45,890,647-47,334,257 , GRCh38 chr19: 45,387,389-46,831,000 CALM3, DMPK, 71 more genes
    nsv3920398copy number variation2nstd102humanUncertain significance NCBI36 chr19: 51,629,587-52,026,097 , GRCh37 chr19: 46,937,747-47,334,257 , GRCh38 chr19: 46,434,490-46,831,000 LOC107987269, GNG8, 16 more genes
    nsv3916206copy number variation1nstd102humanPathogenic GRCh37 chr19: 46,099,131-47,103,283 , NCBI36 chr19: 50,790,971-51,795,123 , GRCh38 chr19: 45,595,873-46,600,026 PNMA8B, MIR642B, 47 more genes
    nsv3910109copy number variation1nstd102humanPathogenic GRCh38 chr19: 46,458,122-47,683,579 , GRCh37 chr19: 46,961,379-48,186,836 , NCBI36 chr19: 51,653,219-52,878,648 FKRP, GNG8, 38 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3900603copy number variation1nstd102humanUncertain significance GRCh37 chr19: 46,918,881-47,782,258 , GRCh38.p12 chr19: 46,415,624-47,279,001 SAE1, ZC3H4, 27 more genes
    nsv3900160copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 46,404,248-48,488,721 , GRCh38.p12 chr19: 45,900,990-47,985,464 C5AR1, CALM3, 84 more genes
    nsv3891669copy number variation1nstd102humanPathogenic GRCh37 chr19: 43,013,365-47,241,534 , GRCh38.p12 chr19: 42,509,213-46,738,277 MIR320E, BCL3, 189 more genes
    esv3883996copy number variation1estd219human GRCh37 chr19: 47,110,442-47,110,509 , GRCh38.p12 chr19: 46,607,185-46,607,252 CALM3
    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