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 252

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099215copy number variation1nstd231human GRCh38.p12 chr1: 84,991,383-97,594,649 , GRCh37 chr1: 85,457,066-98,060,205 ABCA4, BRDT, 220 more genes
    nsv7051476inversion1nstd229human GRCh38 chr1: 87,647,529-89,769,769 , GRCh37.p13 chr1: 88,113,212-90,235,328 RBMXL1, PTGES3P1, 35 more genes
    nsv7046575inversion1nstd229human GRCh38 chr1: 83,069,893-89,051,563 , GRCh37.p13 chr1: 83,535,576-89,517,246 LOC105378826, RN7SL583P, 87 more genes
    nsv6656750copy number variation1nstd229human GRCh38 chr1: 88,890,430-88,894,189 , GRCh37.p13 chr1: 89,356,113-89,359,872 GTF2B
    nsv6656743copy number variation1nstd229human GRCh38 chr1: 88,606,592-88,883,708 , GRCh37.p13 chr1: 89,072,275-89,349,391 RNU6-125P, ELOCP19, 4 more genes
    nsv6656610copy number variation1nstd229human GRCh38 chr1: 88,877,223-88,881,197 , GRCh37.p13 chr1: 89,342,906-89,346,880 GTF2B
    nsv6656607copy number variation1nstd229human GRCh38 chr1: 88,855,272-88,855,364 , GRCh37.p13 chr1: 89,320,955-89,321,047 GTF2B
    nsv6656525copy number variation1nstd229human GRCh38 chr1: 88,864,371-88,877,215 , GRCh37.p13 chr1: 89,330,054-89,342,898 GTF2B
    nsv6656524copy number variation1nstd229human GRCh38 chr1: 88,860,139-88,860,355 , GRCh37.p13 chr1: 89,325,822-89,326,038 GTF2B
    nsv6656523copy number variation1nstd229human GRCh38 chr1: 88,857,244-88,857,504 , GRCh37.p13 chr1: 89,322,927-89,323,187 GTF2B
    nsv6626407copy number variation1nstd224human GRCh37 chr1: 89,265,248-89,322,809 , GRCh38.p12 chr1: 88,799,565-88,857,126 ELOCP19, PKN2, 2 more genes
    nsv6555037inversion1nstd223human GRCh38 chr1: 88,853,523-88,854,462 , GRCh37.p13 chr1: 89,319,206-89,320,145 GTF2B
    nsv6553855inversion1nstd223human GRCh38 chr1: 88,859,068-88,859,644 , GRCh37.p13 chr1: 89,324,751-89,325,327 GTF2B
    nsv6551622inversion1nstd223human GRCh38 chr1: 88,872,482-88,873,489 , GRCh37.p13 chr1: 89,338,165-89,339,172 GTF2B
    nsv6549966inversion1nstd223human GRCh38 chr1: 88,872,154-88,873,520 , GRCh37.p13 chr1: 89,337,837-89,339,203 GTF2B
    nsv6549707inversion1nstd223human GRCh38 chr1: 88,871,747-88,872,456 , GRCh37.p13 chr1: 89,337,430-89,338,139 GTF2B
    nsv6542810inversion1nstd223human GRCh38 chr1: 86,344,314-89,254,085 , GRCh37.p13 chr1: 86,809,997-89,719,768 GBP3, LOC105378838, 52 more genes
    nsv6542421inversion1nstd223human GRCh38 chr1: 85,951,963-92,104,665 , GRCh37.p13 chr1: 86,417,646-92,570,222 LOC105378844, LINC01773, 104 more genes
    nsv6540288inversion1nstd223human GRCh38 chr1: 88,862,282-88,862,939 , GRCh37.p13 chr1: 89,327,965-89,328,622 GTF2B
    nsv6536739inversion1nstd223human GRCh38 chr1: 86,344,291-89,254,074 , GRCh37.p13 chr1: 86,809,974-89,719,757 LOC105378835, RPL7L1P22, 52 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