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 203

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6452016copy number variation1nstd223human GRCh38 chr9: 138,213,701-138,215,100 , GRCh37.p13 chr9: 141,104,151-141,105,550 FAM157B
    nsv6446538copy number variation1nstd223human GRCh38 chr9: 138,216,801-138,217,800 , GRCh37.p13 chr9: 141,107,251-141,108,250 FAM157B
    nsv6445400copy number variation1nstd223human GRCh38 chr9: 138,216,801-138,219,600 , GRCh37.p13 chr9: 141,107,251-141,110,050 FAM157B
    nsv6441282copy number variation1nstd223human GRCh38 chr9: 138,206,201-138,224,500 , GRCh37.p13 chr9: 141,096,651-141,114,950 FAM157B
    nsv6302800copy number variation1nstd186human GRCh37 chr9: 141,123,818-141,136,986 , GRCh38.p12 chr9: 138,233,368-138,246,536 FAM157B
    nsv6266295copy number variation1nstd214human GRCh38 chr9: 138,232,311-138,232,373 , GRCh37.p13 chr9: 141,122,761-141,122,823 FAM157B
    nsv6142084copy number variation1nstd206human GRCh38 chr9: 138,255,468-138,334,600 , GRCh37.p13 chr11: 72,884-113,183 , FAM157B, 6 more genes
    nsv6141946copy number variation1nstd206human GRCh38 chr9: 138,233,368-138,246,536 , GRCh37.p13 chr9: 141,123,818-141,136,986 FAM157B
    nsv6141845copy number variation1nstd206human GRCh38 chr9: 138,177,536-138,223,536 , GRCh37.p13 chr9: 141,071,988-141,113,986 , FAM157B, 2 more genes
    nsv6141791copy number variation1nstd206human GRCh38 chr9: 138,139,536-138,334,600 , GRCh37.p13 chr9: 141,033,988-141,153,431 , FAM157B, 10 more genes
    nsv6141665copy number variation1nstd206human GRCh38 chr9: 138,262,950-138,268,500 , GRCh37.p13 chr1: 148,979-154,500 , FAM157B
    nsv6141484copy number variation1nstd206human GRCh38 chr9: 138,227,536-138,235,536 , GRCh37.p13 chr9: 141,117,986-141,125,986 FAM157B
    nsv6141416copy number variation1nstd206human GRCh38 chr9: 138,139,536-138,259,600 , GRCh37.p13 chr9: 141,033,988-141,150,050 , TUBBP5, 4 more genes
    nsv6137446copy number variation1nstd213human GRCh37 chr9: 138,580,000-141,150,001 , GRCh38.p12 chr9: 135,688,154-138,259,551 ABCA2, C8G, 123 more genes
    nsv6099505insertion1nstd212human GRCh38 chr9: 138,227,894-138,227,894 , GRCh37.p13 chr9: 141,118,344-141,118,344 FAM157B
    nsv6099349insertion1nstd212human GRCh38 chr9: 138,231,525-138,231,525 , GRCh37.p13 chr9: 141,121,975-141,121,975 FAM157B
    nsv6099222insertion1nstd212human GRCh38 chr9: 138,227,968-138,227,968 , GRCh37.p13 chr9: 141,118,418-141,118,418 FAM157B
    nsv6093450insertion1nstd212human GRCh38 chr9: 138,233,051-138,233,051 , GRCh37.p13 chr9: 141,123,501-141,123,501 FAM157B
    nsv6093355insertion1nstd212human GRCh38 chr9: 138,232,746-138,232,746 , GRCh37.p13 chr9: 141,123,196-141,123,196 FAM157B
    nsv6088594insertion1nstd212human GRCh38 chr9: 138,233,137-138,233,137 , GRCh37.p13 chr9: 141,123,587-141,123,587 FAM157B
    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