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 344

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7136954copy number variation1nstd102humanUncertain significance GRCh37 chr15: 31,196,075-31,233,768 , GRCh38.p12 chr15|NT_187660.1: 3,189,604-3,227,294 , GRCh38.p12 chr15: 30,903,872-30,941,565 , GRCh38.p12 chr15|NW_011332701.1: 3,077,152-3,114,842 FAN1, MTMR10
    nsv3914900copy number variation1nstd102humanLikely pathogenic NCBI36 chr7: 5,584,342-5,781,608 , GRCh37 chr7: 5,617,816-5,815,082 , GRCh38 chr7: 5,578,185-5,775,451 FSCN1, RNF216, 2 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 FAN1, H3P40, 1616 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 FAN1, RNU6-18P, 1442 more genes
    nsv3917652copy number variation1nstd102humanPathogenic NCBI36 chr15: 20,249,886-36,169,075 , GRCh38 chr15: 23,319,714-38,089,582 , GRCh37 chr15: 22,698,522-38,381,783 FAN1, LOC105370764, 345 more genes
    nsv4674936copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-36,861,479 , GRCh38.p12 chr15: 23,319,714-36,569,278 FAN1, SNORD115-48, 330 more genes
    nsv3921026copy number variation1nstd102humanPathogenic NCBI36 chr15: 22,830,109-35,283,797 , GRCh38 chr15: 25,033,869-37,204,304 , GRCh37 chr15: 25,279,016-37,496,505 FAN1, SNORD116-17, 303 more genes
    nsv4348926copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,848,750-32,925,141 , GRCh38.p12 chr15: 20,643,448-32,632,940 FAN1, SNORD116-9, 376 more genes
    nsv3882370copy number variation1nstd102humanPathogenic NCBI36 chr15: 19,359,417-30,302,218 , GRCh37.p13 chr15: 21,129,984-32,514,926 , GRCh38.p12 chr15: 20,924,655-32,222,725 FAN1, OR11H3P, 341 more genes
    nsv3913044copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,765,628-32,676,855 , NCBI36 chr15: 20,316,992-30,464,147 , GRCh38 chr15: 23,319,714-32,384,654 FAN1, RNA5SP390, 245 more genes
    nsv4675045copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,213,406-32,446,830 , GRCh38.p12 chr15: 23,319,714-32,154,629 FAN1, SNORD108, 240 more genes
    nsv6634429copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,739,497-28,566,579 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 20,534,259-28,321,433 FAN1, OR11J7P, 364 more genes
    nsv6315542copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,285,775-30,386,399 , GRCh38.p12 chr15: 23,319,714-30,094,196 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 FAN1, RPL5P1, 247 more genes
    nsv3894238copy number variation2nstd102humanPathogenic GRCh37 chr15: 22,770,421-30,386,398 , GRCh38.p12 chr15: 23,319,714-30,094,195 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 FAN1, SNORD115-28, 247 more genes
    nsv6315525copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-29,855,014 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-29,562,810 FAN1, SNORD115-37, 247 more genes
    nsv3920006copy number variation1nstd102humanPathogenic GRCh37 chr7: 45,130-5,920,006 , GRCh38 chr7: 45,130-5,880,375 , NCBI36 chr7: 140,213-5,886,532 RNU6-215P, NUDT1, 120 more genes
    nsv3905892copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-29,069,001 , GRCh38.p12 chr15: 23,319,714-28,823,855 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 FAN1, SNORD115-10, 247 more genes
    nsv3908078copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,288,374-29,062,203 , GRCh38.p12 chr15: 23,319,714-28,817,057 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 FAN1, GOLGA6L7, 247 more genes
    nsv3906002copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-29,062,203 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,817,057 FAN1, PWRN1, 247 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