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 367

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099252copy number variation1nstd231human GRCh38.p12 chr1: 179,130,308-181,685,140 , GRCh37 chr1: 179,099,443-181,654,276 ABL2, CACNA1E, 48 more genes
    nsv7051410inversion1nstd229human GRCh38 chr1: 180,227,889-180,230,645 , GRCh37.p13 chr1: 180,197,024-180,199,780 LHX4
    nsv6645747copy number variation1nstd229human GRCh38 chr1: 180,200,301-180,231,200 , GRCh37.p13 chr1: 180,169,436-180,200,335 LHX4, QSOX1
    nsv6645744copy number variation1nstd229human GRCh38 chr1: 180,054,518-180,252,685 , GRCh37.p13 chr1: 180,023,653-180,221,820 LOC105371636, CEP350, 2 more genes
    nsv6645697copy number variation1nstd229human GRCh38 chr1: 180,279,461-180,289,673 , GRCh37.p13 chr1: 180,248,596-180,258,808 LHX4, ACBD6
    nsv6645604copy number variation1nstd229human GRCh38 chr1: 180,279,300-180,280,033 , GRCh37.p13 chr1: 180,248,435-180,249,168 ACBD6, LHX4
    nsv6645603copy number variation1nstd229human GRCh38 chr1: 180,259,338-180,261,320 , GRCh37.p13 chr1: 180,228,473-180,230,455 LHX4
    nsv6645602copy number variation1nstd229human GRCh38 chr1: 180,258,486-180,258,860 , GRCh37.p13 chr1: 180,227,621-180,227,995 LHX4
    nsv6645223copy number variation1nstd229human GRCh38 chr1: 180,259,701-180,261,500 , GRCh37.p13 chr1: 180,228,836-180,230,635 LHX4
    nsv6645222copy number variation1nstd229human GRCh38 chr1: 180,259,340-180,261,269 , GRCh37.p13 chr1: 180,228,475-180,230,404 LHX4
    nsv6645220copy number variation1nstd229human GRCh38 chr1: 180,176,158-180,301,960 , GRCh37.p13 chr1: 180,145,293-180,271,095 LHX4-AS1, QSOX1, 2 more genes
    nsv6637124copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,727,182-192,260,142 , GRCh38.p12 chr1: 179,758,047-192,291,012 LOC101928933, KIAA1614-AS1, 148 more genes
    nsv6538365inversion1nstd223human GRCh38 chr1: 178,815,320-184,820,865 , GRCh37.p13 chr1: 178,784,455-184,789,999 NPHS2, COLGALT2, 111 more genes
    nsv6329132copy number variation1nstd223human GRCh38 chr1: 180,255,460-180,256,439 , GRCh37.p13 chr1: 180,224,595-180,225,574 LHX4
    nsv6324776copy number variation1nstd223human GRCh38 chr1: 180,258,601-180,261,400 , GRCh37.p13 chr1: 180,227,736-180,230,535 LHX4
    nsv6322628copy number variation1nstd223human GRCh38 chr1: 180,179,735-180,240,644 , GRCh37.p13 chr1: 180,148,870-180,209,779 QSOX1, LHX4
    nsv6318478copy number variation1nstd223human GRCh38 chr1: 180,006,276-180,725,862 , GRCh37.p13 chr1: 179,975,411-180,694,998 LHX4-AS1, LOC105371637, 9 more genes
    nsv6318372copy number variation1nstd223human GRCh38 chr1: 180,232,492-180,233,725 , GRCh37.p13 chr1: 180,201,627-180,202,860 LHX4
    nsv6310922copy number variation1nstd102humanUncertain significance GRCh37 chr1: 179,520,308-183,559,464 , GRCh38.p12 chr1: 179,551,173-183,590,329 NMNAT2, FAM163A, 78 more genes
    nsv6290451copy number variation1nstd102humanPathogenic GRCh37 chr1: 178,522,021-190,322,133 , GRCh38.p12 chr1: 178,552,886-190,353,003 RNU7-13P, LOC105371642, 167 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