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 244

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142343copy number variation1nstd232human GRCh37.p13 chr1: 171,179,940-171,180,020 , GRCh38.p12 chr1: 171,210,801-171,210,881 FMO2, LOC105371611
    nsv7099246copy number variation1nstd231human GRCh38.p12 chr1: 170,327,769-171,350,588 , GRCh37 chr1: 170,296,910-171,319,727 FMO1, FMO2, 16 more genes
    nsv7056561inversion1nstd229human GRCh38 chr1: 171,183,850-171,183,876 , GRCh37.p13 chr1: 171,152,989-171,153,015 LOC105371611, FMO2
    nsv6644572copy number variation1nstd229human GRCh38 chr1: 171,211,550-171,211,770 , GRCh37.p13 chr1: 171,180,689-171,180,909 FMO2, LOC105371611
    nsv6644569copy number variation1nstd229human GRCh38 chr1: 171,089,340-171,371,617 , GRCh37.p13 chr1: 171,058,481-171,340,756 FMO3, MIR1295A, 9 more genes
    nsv6644534copy number variation1nstd229human GRCh38 chr1: 171,187,292-171,212,720 , GRCh37.p13 chr1: 171,156,431-171,181,859 FMO2, LOC105371611
    nsv6644455copy number variation1nstd229human GRCh38 chr1: 171,210,792-171,217,463 , GRCh37.p13 chr1: 171,179,931-171,186,602 FMO2, LOC105371611
    nsv6644453copy number variation1nstd229human GRCh38 chr1: 171,117,583-171,372,251 , GRCh37.p13 chr1: 171,086,723-171,341,390 FMO2, SRP14P4, 7 more genes
    nsv6644080copy number variation1nstd229human GRCh38 chr1: 171,207,601-171,210,600 , GRCh37.p13 chr1: 171,176,740-171,179,739 FMO2, LOC105371611
    nsv6644079copy number variation1nstd229human GRCh38 chr1: 171,193,523-171,196,646 , GRCh37.p13 chr1: 171,162,662-171,165,785 FMO2, LOC105371611
    nsv6625809copy number variation1nstd224human GRCh37 chr1: 171,019,772-171,350,357 , GRCh38.p12 chr1: 171,050,631-171,381,218 FMO1, FMO4, 11 more genes
    nsv6328233copy number variation1nstd223human GRCh38 chr1: 171,211,550-171,211,770 , GRCh37.p13 chr1: 171,180,689-171,180,909 FMO2, LOC105371611
    nsv6327103copy number variation1nstd223human GRCh38 chr1: 171,213,160-171,213,946 , GRCh37.p13 chr1: 171,182,299-171,183,085 FMO2, LOC105371611
    nsv6325393copy number variation1nstd223human GRCh38 chr1: 171,190,217-171,191,176 , GRCh37.p13 chr1: 171,159,356-171,160,315 LOC105371611, FMO2
    nsv6319327copy number variation1nstd223human GRCh38 chr1: 171,193,523-171,195,989 , GRCh37.p13 chr1: 171,162,662-171,165,128 LOC105371611, FMO2
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 LOC100420658, LOC105371610, 167 more genes
    nsv6313602copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,391,422-171,843,613 , GRCh38.p12 chr1: 167,422,185-171,874,473 DCAF6, SELE, 101 more genes
    nsv6245602mobile element insertion1nstd215human GRCh38 chr1: 171,187,245-171,187,245 , GRCh37.p13 chr1: 171,156,384-171,156,384 FMO2, LOC105371611
    nsv6158263copy number variation1nstd214human GRCh38 chr1: 171,210,801-171,210,881 , GRCh37.p13 chr1: 171,179,940-171,180,020 LOC105371611, FMO2
    nsv6151323copy number variation1nstd214human GRCh38 chr1: 171,210,755-171,210,833 , GRCh37.p13 chr1: 171,179,894-171,179,972 FMO2, LOC105371611
    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