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 294

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7082318copy number variation1nstd229human GRCh38 chrX: 110,519,762-110,544,104 , GRCh37.p13 chrX: 109,762,990-109,787,332 CRIPTO3
    nsv7082317copy number variation1nstd229human GRCh38 chrX: 110,516,749-110,519,655 , GRCh37.p13 chrX: 109,759,977-109,762,883 CRIPTO3
    esv2986071insertion1estd209human GRCh37 chrX: 109,763,925-109,763,925 , GRCh38.p12 chrX: 110,520,697-110,520,697 CRIPTO3
    esv1525593insertion1estd22human NCBI36 chrX: 109,650,592-109,650,592 , GRCh37.p13 chrX: 109,763,936-109,763,936 , GRCh38.p12 chrX: 110,520,708-110,520,708 CRIPTO3
    esv1366168insertion1estd22human NCBI36 chrX: 109,652,809-109,652,809 , GRCh37.p13 chrX: 109,766,153-109,766,153 , GRCh38.p12 chrX: 110,522,925-110,522,925 CRIPTO3
    esv1036526insertion1estd22human NCBI36 chrX: 109,649,530-109,649,530 , GRCh37.p13 chrX: 109,762,874-109,762,874 , GRCh38.p12 chrX: 110,519,646-110,519,646 CRIPTO3
    nsv2716540short tandem repeat6nstd128human GRCh37 chrX: 109,766,137-109,766,158 , GRCh38.p12 chrX: 110,522,909-110,522,930 CRIPTO3
    nsv2682394short tandem repeat8nstd128human GRCh37 chrX: 109,762,856-109,762,874 , GRCh38.p12 chrX: 110,519,628-110,519,646 CRIPTO3
    nsv2716539short tandem repeat1nstd128human GRCh37 chrX: 109,762,178-109,762,194 , GRCh38.p12 chrX: 110,518,950-110,518,966 CRIPTO3
    nsv3896905copy number variation1nstd102humanUncertain significance GRCh37 chrX: 109,693,720-110,244,649 , NCBI36 chrX: 109,580,376-110,131,305 , GRCh38 chrX: 110,450,492-111,001,421 PAK3, CRIPTO3, 3 more genes
    nsv4674780copy number variation1nstd102humanPathogenic GRCh37 chrX: 109,418,639-110,180,983 , GRCh38.p12 chrX: 110,175,411-110,937,755 CRIPTO3, AMMECR1, 7 more genes
    nsv3874664copy number variation1nstd102humanPathogenic GRCh38 chrX: 110,250,890-110,665,082 , GRCh37.p13 chrX: 109,494,118-109,908,310 CRIPTO3, AMMECR1, 4 more genes
    nsv3904162copy number variation1nstd102humanPathogenic GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754 NANOGNBP3, PRXL2CP1, 2154 more genes
    nsv3913255copy number variation2nstd102humanPathogenic NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895 NHS-AS1, DUSP21, 2154 more genes
    nsv3907094copy number variation4nstd102humanPathogenic GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065 GPR119, RN7SKP81, 2153 more genes
    nsv3878553copy number variation2nstd102humanPathogenic GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100 H2AB2, RTL3, 2152 more genes
    nsv3898149copy number variation1nstd102humanPathogenic GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792 OR3B1P, SSX4B, 2154 more genes
    nsv3877395copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174 ARMCX2, RNA5SP505, 2154 more genes
    nsv3884935copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127 NDUFB11, VN1R110P, 2154 more genes
    nsv3903061copy number variation1nstd102humanPathogenic NCBI36 chrX: 679-154,896,026 , GRCh38 chrX: 10,679-156,013,167 , GRCh37 chrX: 60,679-155,242,832 SLC38A5, CT45A1, 2152 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