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 484

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098440copy number variation1nstd102humanUncertain significance GRCh37 chr9: 140,036,445-140,138,008 , GRCh38.p12 chr9: 137,141,993-137,243,556 SSNA1, CYSRT1, 14 more genes
    nsv7098071copy number variation2nstd102humanPathogenic GRCh37 chr9: 139,089,171-141,016,451 , GRCh38.p12 chr9: 136,197,325-138,121,999 NPDC1, LOC101928786, 108 more genes
    nsv7098070copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,392,557-141,016,451 , GRCh38.p12 chr9: 135,500,711-138,121,999 STPG3-AS1, CACNA1B-AS1, 132 more genes
    nsv7097938copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 140,040,158-141,016,451 , GRCh38.p12 chr9: 137,145,706-138,121,999 NELFB, LOC651337, 39 more genes
    nsv7097697copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,218,768-141,016,451 , GRCh38.p12 chr9: 133,351,913-138,121,999 LOC105376326, LOC107987143, 186 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7093414copy number variation1nstd102humanPathogenic GRCh38 chr9: 134,932,722-137,269,957 , GRCh37.p13 chr9: 137,824,568-140,164,409 LHX3, FUT7, 121 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv6897081copy number variation1nstd229human GRCh38 chr9: 137,175,201-137,279,700 , GRCh37.p13 chr9: 140,069,653-140,174,152 SLC34A3, TOR4A, 13 more genes
    nsv6887834copy number variation1nstd229human GRCh38 chr9: 137,194,602-137,210,908 , GRCh37.p13 chr9: 140,089,054-140,105,360 TMEM203, TPRN, 1 more genes
    nsv6879141copy number variation1nstd229human GRCh38 chr9: 137,145,000-137,226,807 , GRCh37.p13 chr9: 140,039,452-140,121,259 LOC105376328, NDOR1, 11 more genes
    nsv6633594copy number variation3nstd224human GRCh37 chr9: 140,087,121-140,099,685 , GRCh38.p12 chr9: 137,192,669-137,205,233 TMEM203, NDOR1, 1 more genes
    nsv6633593copy number variation1nstd224human GRCh37 chr9: 140,086,956-140,108,261 , GRCh38.p12 chr9: 137,192,504-137,213,809 TMEM203, NDOR1, 1 more genes
    nsv6633592copy number variation2nstd224human GRCh37 chr9: 140,063,557-140,108,448 , GRCh38.p12 chr9: 137,169,105-137,213,996 GRIN1, SSNA1, 7 more genes
    nsv6633164copy number variation1nstd224human GRCh37 chr9: 140,093,452-140,108,261 , GRCh38.p12 chr9: 137,199,000-137,213,809 NDOR1, TPRN, 1 more genes
    nsv6633163copy number variation1nstd224human GRCh37 chr9: 140,082,971-140,099,685 , GRCh38.p12 chr9: 137,188,519-137,205,233 NDOR1, TPRN, 3 more genes
    nsv6450572copy number variation1nstd223human GRCh38 chr9: 135,800,101-137,359,000 , GRCh37.p13 chr9: 138,691,947-140,253,452 LCN6, PAXX, 96 more genes
    nsv6448504copy number variation1nstd223human GRCh38 chr9: 135,900,001-137,301,100 , GRCh37.p13 chr9: 138,791,847-140,195,552 DIPK1B, LOC105376326, 95 more genes
    nsv6313986copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,563,039-140,310,033 , GRCh38.p12 chr9: 136,668,587-137,415,581 RABL6, ANAPC2, 68 more genes
    nsv6313935copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,740,078-141,020,389 , GRCh38.p12 chr9: 135,848,232-138,125,937 ENTR1, LINC02692, 115 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