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 132

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5381271copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,762,699-3,808,981 , GRCh38.p12 chr19: 3,762,701-3,808,983 MATK, RAX2, 3 more genes
    nsv5294162copy number variation1nstd204human GRCh38.p13 chr19: 3,332,801-3,820,800 , GRCh37.p13 chr19: 3,332,799-3,820,798 LOC105372245, LOC105372248, 19 more genes
    nsv5292408copy number variation1nstd204human GRCh38.p13 chr19: 2,552,101-4,875,100 , GRCh37.p13 chr19: 2,552,099-4,875,112 , S1PR4, 93 more genes
    nsv5014359copy number variation1nstd200human GRCh38 chr19: 3,754,009-3,782,407 , GRCh37.p13 chr19: 3,754,007-3,782,405 APBA3, RAX2, 3 more genes
    nsv4864831copy number variation1nstd200human GRCh37 chr19: 3,754,007-3,782,405 , GRCh38.p12 chr19: 3,754,009-3,782,407 LOC105372248, RAX2, 3 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MRPL54, DAZAP1, 198 more genes
    nsv4535913copy number variation1nstd166human GRCh37.p13 chr19: 3,771,312-3,771,835 , GRCh38.p12 chr19: 3,771,314-3,771,837 RAX2
    nsv4457843copy number variation1nstd102humanUncertain significance GRCh37 chr19: 3,132,909-3,907,470 , GRCh38.p12 chr19: 3,132,911-3,907,472 LOC105372244, TEKTIP1, 27 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 BSG, LOC100420586, 217 more genes
    nsv4436611copy number variation1nstd102humanUncertain significance GRCh37 chr19: 2,229,488-4,004,142 , GRCh38.p12 chr19: 2,229,489-4,004,144 LMNB2, SF3A2, 76 more genes
    nsv4350537copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,076,808-4,796,782 , GRCh38.p12 chr19: 3,076,810-4,796,770 FEM1A, MIR7-3, 70 more genes
    nsv4264293copy number variation1nstd166human GRCh37.p13 chr19: 3,760,122-3,810,544 , GRCh38.p12 chr19: 3,760,124-3,810,546 MATK, APBA3, 4 more genes
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 POLR2E, PWWP3A, 283 more genes
    nsv3923561copy number variation1nstd102humanPathogenic NCBI36 chr19: 184,565-4,650,484 , GRCh37 chr19: 233,565-4,699,484 , GRCh38 chr19: 233,565-4,699,472 DAPK3, IZUMO4, 214 more genes
    nsv3921957copy number variation1nstd102humanPathogenic GRCh38 chr19: 2,926,238-4,051,635 , NCBI36 chr19: 2,877,236-4,002,633 , GRCh37 chr19: 2,926,236-4,051,633 TEKTIP1, APBA3, 42 more genes
    nsv3915373copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,516,574-4,059,126 , GRCh37 chr19: 1,565,574-4,108,126 , GRCh38 chr19: 1,565,575-4,108,128 LOC100419704, DIRAS1, 104 more genes
    nsv3915152copy number variation1nstd102humanPathogenic NCBI36 chr19: 3,289,022-4,784,151 , GRCh38 chr19: 3,338,024-4,833,139 , GRCh37 chr19: 3,338,022-4,833,151 APBA3, TEKTIP1, 63 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 SEMA6B, RANBP3-DT, 299 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