U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 28

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3901061copy number variation1nstd102humanUncertain significance GRCh37 chr19: 3,783,813-3,834,742 , GRCh38.p12 chr19: 3,783,815-3,834,744 MATK, ZFR2
    nsv3899349copy number variation1nstd102humanconflicting data from submitters GRCh37 chr19: 3,801,763-3,834,742 , GRCh38.p12 chr19: 3,801,765-3,834,744 MATK, ZFR2
    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
    nsv3910710copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,549,143-4,288,717 , NCBI36 chr19: 1,500,143-4,239,717 , GRCh38 chr19: 1,549,144-4,288,720 MATK, EBI3, 110 more genes
    nsv6291587copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,501,624-5,357,124 , GRCh38.p12 chr19: 3,501,626-5,357,113 MATK, RN7SL202P, 67 more genes
    nsv4350537copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,076,808-4,796,782 , GRCh38.p12 chr19: 3,076,810-4,796,770 MATK, FEM1A, 70 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 MATK, APBA3, 63 more genes
    nsv3910627copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,554,633-4,690,977 , NCBI36 chr19: 3,505,633-4,641,977 , GRCh38 chr19: 3,554,635-4,690,965 MATK, PIAS4, 49 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 MATK, TEKTIP1, 42 more genes
    nsv3912343copy number variation1nstd102humanPathogenic NCBI36 chr19: 3,388,994-3,990,215 , GRCh38 chr19: 3,437,996-4,039,217 , GRCh37 chr19: 3,437,994-4,039,215 MATK, FZR1, 28 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 MATK, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 MATK, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 MATK, LENG8, 2408 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 MATK, SEMA6B, 299 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 MATK, POLR2E, 283 more genes
    nsv3890584copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144 MATK, PCP2, 250 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 MATK, BSG, 217 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 MATK, DAPK3, 214 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MATK, MRPL54, 198 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 MATK, LOC100419704, 104 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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