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 263

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099297copy number variation1nstd231human GRCh38.p12 chr1: 58,444,770-67,143,664 , GRCh37 chr1: 58,910,442-67,609,347 AK4, CYP2J2, 125 more genes
    nsv7099208copy number variation1nstd231human GRCh38.p12 chr1: 59,526,542-66,009,490 , GRCh37 chr1: 59,992,214-66,475,173 AK4, CYP2J2, 96 more genes
    nsv7096059copy number variation1nstd102humanUncertain significance GRCh37 chr1: 65,299,551-65,351,947 , GRCh38.p12 chr1: 64,833,868-64,886,264 JAK1, RAVER2
    nsv7095627copy number variation1nstd102humanPathogenic GRCh37 chr1: 61,548,464-67,861,772 , GRCh38.p12 chr1: 61,082,792-67,396,089 ALG6, MIR3116-2, 94 more genes
    nsv7095538copy number variation1nstd102humanPathogenic GRCh37 chr1: 65,299,551-67,861,772 , GRCh38.p12 chr1: 64,833,868-67,396,089 MRPS21P1, MIER1, 36 more genes
    nsv6653408copy number variation1nstd229human GRCh38 chr1: 64,792,601-64,794,600 , GRCh37.p13 chr1: 65,258,284-65,260,283 RAVER2
    nsv6653407copy number variation1nstd229human GRCh38 chr1: 64,784,646-64,802,622 , GRCh37.p13 chr1: 65,250,329-65,268,305 RAVER2
    nsv6653406copy number variation1nstd229human GRCh38 chr1: 64,761,140-64,761,340 , GRCh37.p13 chr1: 65,226,823-65,227,023 RAVER2
    nsv6653188copy number variation1nstd229human GRCh38 chr1: 64,804,251-64,805,385 , GRCh37.p13 chr1: 65,269,934-65,271,068 RAVER2
    nsv6653187copy number variation1nstd229human GRCh38 chr1: 64,786,212-64,787,331 , GRCh37.p13 chr1: 65,251,895-65,253,014 RAVER2
    nsv6653090copy number variation1nstd229human GRCh38 chr1: 64,756,433-64,758,922 , GRCh37.p13 chr1: 65,222,116-65,224,605 RAVER2
    nsv6652659copy number variation1nstd229human GRCh38 chr1: 64,778,548-64,780,217 , GRCh37.p13 chr1: 65,244,231-65,245,900 RAVER2
    nsv6652658copy number variation1nstd229human GRCh38 chr1: 64,773,201-64,775,100 , GRCh37.p13 chr1: 65,238,884-65,240,783 RAVER2
    nsv6549812inversion1nstd223human GRCh38 chr1: 64,823,825-64,824,787 , GRCh37.p13 chr1: 65,289,508-65,290,470 RAVER2
    nsv6546625inversion1nstd223human GRCh38 chr1: 64,824,035-64,824,648 , GRCh37.p13 chr1: 65,289,718-65,290,331 RAVER2
    nsv6542115inversion1nstd223human GRCh38 chr1: 61,925,268-71,371,290 , GRCh37.p13 chr1: 62,390,940-71,836,973 PATJ, GNG12-AS1, 142 more genes
    nsv6538284inversion1nstd223human GRCh38 chr1: 64,801,296-64,801,444 , GRCh37.p13 chr1: 65,266,979-65,267,127 RAVER2
    nsv6335426copy number variation1nstd223human GRCh38 chr1: 64,770,901-64,772,500 , GRCh37.p13 chr1: 65,236,584-65,238,183 RAVER2
    nsv6333652copy number variation1nstd223human GRCh38 chr1: 64,775,971-64,788,461 , GRCh37.p13 chr1: 65,241,654-65,254,144 RAVER2
    nsv6332975copy number variation1nstd223human GRCh38 chr1: 64,788,667-64,793,594 , GRCh37.p13 chr1: 65,254,350-65,259,277 RAVER2
    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