U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from BioSample

Items: 1 to 20 of 3172

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4684017copy number variation142nstd187human GRCh37 chr8: 6,872,895-6,876,338 , GRCh38.p12 chr8: 7,015,373-7,018,816 , GRCh38.p12 chr8|NW_018654717.1: 410,494-413,940 DEFA3
    esv3817218delins1586estd214human GRCh37 chrX: 1,018,298-1,018,298 , GRCh38.p12 chrX: 1,057,563-1,057,563 0
    esv3817884copy number variation1789estd214human GRCh37 chrX: 131,089,382-131,089,611 , GRCh38.p12 chrX: 131,955,354-131,955,583 0
    esv3817610mobile element insertion1552estd214human GRCh37 chrX: 126,290,693-126,290,693 , GRCh38.p12 chrX: 127,156,710-127,156,710 0
    esv3817887mobile element insertion275estd214human GRCh37 chrX: 95,537,355-95,537,355 , GRCh38.p12 chrX: 96,282,356-96,282,356 0
    esv3817633copy number variation942estd214human GRCh37 chrX: 153,733,758-153,734,289 , GRCh38.p12 chrX: 154,505,427-154,505,958 FAM3A
    esv3817154copy number variation887estd214human GRCh37 chrX: 32,886,342-32,886,931 , GRCh38.p12 chrX: 32,868,225-32,868,814 DMD
    esv3817825copy number variation514estd214human GRCh37 chrX: 110,094,444-110,095,367 , GRCh38.p12 chrX: 110,851,216-110,852,139 0
    esv3817191copy number variation775estd214human GRCh37 chrX: 153,634,830-153,636,529 , GRCh38.p12 chrX: 154,406,489-154,408,193 DNASE1L1
    esv3817378mobile element insertion32estd214human GRCh37 chrX: 63,440,816-63,440,816 , GRCh38.p12 chrX: 64,220,936-64,220,936 0
    esv3817752copy number variation714estd214human GRCh37 chrX: 53,819,537-53,820,304 , GRCh38.p12 chrX: 53,793,039-53,793,806
    esv3816956copy number variation1245estd214human GRCh37 chrX: 97,167,898-97,168,316 , GRCh38.p12 chrX: 97,912,900-97,913,318 0
    esv3817436copy number variation215estd214human GRCh37 chrX: 94,577,293-94,578,659 , GRCh38.p12 chrX: 95,322,294-95,323,660 0
    esv3817025copy number variation869estd214human GRCh37 chrX: 105,581,825-105,582,814 , GRCh38.p12 chrX: 106,338,596-106,339,585 0
    esv3817694copy number variation502estd214human GRCh37 chrX: 24,184,245-24,185,065 , GRCh38.p12 chrX: 24,166,128-24,166,948 ZFX
    esv3817515copy number variation60estd214human GRCh37 chrX: 53,477,093-53,492,686 , GRCh38.p12 chrX: 53,450,145-53,465,741 VTRNA3-1P, TIPINP1
    esv3817250copy number variation1086estd214human GRCh37 chrX: 80,572,069-80,573,144 , GRCh38.p12 chrX: 81,316,570-81,317,645 0
    esv3817829copy number variation603estd214human GRCh37 chrX: 48,500,496-48,502,930 , GRCh38.p12 chrX: 48,642,108-48,644,542 0
    esv3817153copy number variation667estd214human GRCh37 chrX: 53,481,170-53,482,871 , GRCh38.p12 chrX: 53,454,223-53,455,924 TIPINP1
    esv3817661copy number variation1165estd214human GRCh37 chrX: 154,778,170-154,778,667 , GRCh38.p12 chrX: 155,548,509-155,549,006 TMLHE
    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