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 206

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919160copy number variation1nstd209human GRCh38 chr9: 131,106,466-131,106,601 , GRCh37.p13 chr9: 133,981,853-133,981,988 AIF1L
    nsv5633346insertion1nstd207human GRCh38 chr9: 131,096,449-131,096,449 , GRCh37.p13 chr9: 133,971,836-133,971,836 AIF1L
    nsv5484924copy number variation1nstd206human GRCh38 chr9: 131,115,734-131,116,032 , GRCh37.p13 chr9: 133,991,121-133,991,419 AIF1L
    nsv5373147translocation1nstd200human GRCh38 chr9: 131,108,117-131,108,117 , GRCh38 chr9: 131,108,238-131,108,238 , GRCh37.p13 chr9: 133,983,625-133,983,625 , GRCh37.p13 chr9: 133,983,504-133,983,504 AIF1L
    nsv4985782copy number variation1nstd200human GRCh38 chr9: 131,106,460-131,110,081 , GRCh37.p13 chr9: 133,981,847-133,985,468 AIF1L
    nsv4729623copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,860,060-134,187,480 , GRCh38.p12 chr9: 130,984,673-131,312,093 RNU6-881P, NUP214, 4 more genes
    nsv4681157copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,540,031-134,398,503 , GRCh38.p12 chr9: 130,664,644-131,523,116 LOC105376299, FIBCD1-AS1, 19 more genes
    nsv4609683copy number variation1nstd183human GRCh37 chr9: 133,860,261-134,016,960 , GRCh38.p12 chr9: 130,984,874-131,141,573 AIF1L, LAMC3, 2 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4435642copy number variation1nstd172human GRCh37.p13 chr9: 133,977,025-133,982,301 , GRCh38.p12 chr9: 131,101,638-131,106,914 AIF1L
    nsv4349353copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 131,670,024-134,514,071 , GRCh38.p12 chr9: 128,907,745-131,638,684 ABL1, ASS1, 69 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4185006copy number variation1nstd166human GRCh37.p13 chr9: 133,988,351-133,988,766 , GRCh38.p12 chr9: 131,112,964-131,113,379 AIF1L
    nsv4173149copy number variation1nstd166human GRCh37.p13 chr9: 133,983,504-133,983,625 , GRCh38.p12 chr9: 131,108,117-131,108,238 AIF1L
    nsv3963591insertion1nstd168human GRCh38 chr9: 131,119,153-131,146,596 , GRCh37.p13 chr9: 133,994,540-134,021,983 NUP214, AIF1L, 1 more genes
    nsv3936576insertion1nstd167human GRCh37 chr9: 133,971,808-133,971,808 , GRCh38.p12 chr9: 131,096,421-131,096,421 AIF1L
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
    nsv3920829copy number variation1nstd102humanPathogenic GRCh38 chr9: 121,112,395-138,075,224 , GRCh37 chr9: 123,874,673-140,969,676 , NCBI36 chr9: 122,914,494-140,089,497 LOC101928786, NRON, 495 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