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 126

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148263copy number variation1nstd102humanPathogenic GRCh38 chr9: 102,995,214-108,903,040 , GRCh37.p13 chr9: 105,757,496-111,665,320 ACTL7B, OR13C3, 88 more genes
    nsv7075258inversion1nstd229human GRCh38 chr9: 105,659,939-106,272,714 , GRCh37.p13 chr9: 108,422,220-109,034,995 LOC107987107, TMEM38B, 6 more genes
    nsv7071806inversion1nstd229human GRCh38 chr9: 105,659,830-105,919,918 , GRCh37.p13 chr9: 108,422,111-108,682,199 DEPDC1P2, TAL2, 4 more genes
    nsv7062784inversion1nstd229human GRCh38 chr9: 105,247,017-105,897,262 , GRCh37.p13 chr9: 108,009,298-108,659,543 SLC44A1, RALGAPA1P1, 9 more genes
    nsv6873240copy number variation1nstd229human GRCh38 chr9: 105,803,704-105,894,916 , GRCh37.p13 chr9: 108,565,985-108,657,197 SLC25A6P5
    nsv6863610copy number variation1nstd229human GRCh38 chr9: 105,773,118-105,968,206 , GRCh37.p13 chr9: 108,535,399-108,730,487 LOC107987108, SLC25A6P5, 1 more genes
    nsv6858468copy number variation1nstd229human GRCh38 chr9: 105,850,811-105,931,561 , GRCh37.p13 chr9: 108,613,092-108,693,842 LOC107987108, SLC25A6P5
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6441179copy number variation1nstd223human GRCh38 chr9: 105,773,118-105,968,203 , GRCh37.p13 chr9: 108,535,399-108,730,484 SLC25A6P5, LOC107987108, 1 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6290765copy number variation1nstd102humanUncertain significance GRCh37 chr9: 102,858,276-110,624,997 , GRCh38.p12 chr9: 100,095,994-107,862,716 RNF20, SMC2, 120 more genes
    nsv6136630copy number variation1nstd213human GRCh37 chr9: 108,290,000-109,010,001 , GRCh38.p12 chr9: 105,527,719-106,247,720 TMEM38B, DEPDC1P2, 10 more genes
    nsv5969274inversion1nstd209human GRCh38 chr9: 105,764,038-105,982,494 , GRCh37.p13 chr9: 108,526,319-108,744,775 TMEM38B, SLC25A6P5, 1 more genes
    nsv5700500mobile element insertion1nstd211human GRCh38 chr9: 105,849,112-105,849,112 , GRCh37.p13 chr9: 108,611,393-108,611,393 SLC25A6P5
    nsv5474451copy number variation1nstd206human GRCh38 chr9: 105,810,065-106,511,699 , GRCh37.p13 chr9: 108,572,346-109,273,980 , SLC25A6P5, 2 more genes
    nsv5405079mobile element insertion1nstd206human GRCh38 chr9: 105,849,112-105,849,163 , GRCh37.p13 chr9: 108,611,393-108,611,444 SLC25A6P5
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983002copy number variation1nstd200human GRCh38 chr9: 105,851,068-105,851,130 , GRCh37.p13 chr9: 108,613,349-108,613,411 SLC25A6P5
    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