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 112

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5020443copy number variation1nstd200human GRCh38 chr19: 35,119,450-35,123,819 , GRCh37.p13 chr19: 35,610,354-35,614,723 LGI4, FXYD3, 1 more genes
    nsv4868168copy number variation1nstd200human GRCh37 chr19: 35,610,354-35,614,723 , GRCh38.p12 chr19: 35,119,450-35,123,819 MIR6887, LGI4, 1 more genes
    nsv4674329copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,553,425-36,264,299 , GRCh38.p12 chr19: 35,062,521-35,773,397 LOC105372379, LSR, 50 more genes
    nsv4457800copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,613,953-36,183,886 , GRCh38.p12 chr19: 35,123,049-35,692,984 SBSN, UPK1A, 38 more genes
    nsv4457758copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,548,527-35,772,471 , GRCh38.p12 chr19: 35,057,623-35,281,568 LOC105372379, LSR, 15 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
    nsv4350190copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,043,556-36,316,644 , GRCh38.p12 chr19: 34,552,651-35,825,742 SCN1B, ETV2, 76 more genes
    nsv4349605copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090 ATP4A, RNY5P10, 129 more genes
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 UBA2, ZNF529, 241 more genes
    nsv3918197copy number variation1nstd102humanPathogenic GRCh38 chr19: 31,367,353-35,417,098 , NCBI36 chr19: 36,550,099-40,599,840 , GRCh37 chr19: 31,858,259-35,908,000 LINC01531, FXYD5, 110 more genes
    nsv3916007copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990 MAG, RNU6-967P, 238 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 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
    nsv3900139copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,735,448-36,120,396 , GRCh38.p12 chr19: 30,244,541-35,629,494 ZNF599, FAM187B2P, 130 more genes
    nsv3897154copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,612,084-35,622,065 , GRCh38.p12 chr19: 35,121,180-35,131,161 FXYD3, MIR6887, 1 more genes
    nsv3896985copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,612,084-35,617,093 , GRCh38.p12 chr19: 35,121,180-35,126,189 LGI4, FXYD3, 1 more genes
    nsv3168446copy number variation1nstd158human GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499 , ACTN4, 449 more genes
    nsv3167559copy number variation1nstd151human GRCh37 chr19: 35,523,429-35,655,153 , GRCh38.p12 chr19: 35,032,525-35,164,250 MIR6887, HPN-AS1, 9 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