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 94

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5910122copy number variation1nstd209human GRCh38 chr9: 125,234,552-125,234,605 , GRCh37.p13 chr9: 127,996,831-127,996,884 HSPA5, RABEPK
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4985710copy number variation1nstd200human GRCh38 chr9: 125,232,008-125,255,390 , GRCh37.p13 chr9: 127,994,287-128,017,669 HSPA5-DT, HSPA5, 1 more genes
    nsv4983636copy number variation1nstd200human GRCh38 chr9: 125,241,097-125,241,937 , GRCh37.p13 chr9: 128,003,376-128,004,216 HSPA5, HSPA5-DT
    nsv4983635copy number variation1nstd200human GRCh38 chr9: 125,232,658-125,234,200 , GRCh37.p13 chr9: 127,994,937-127,996,479 HSPA5, RABEPK
    nsv4983634copy number variation1nstd200human GRCh38 chr9: 125,232,700-125,233,645 , GRCh37.p13 chr9: 127,994,979-127,995,924 HSPA5, RABEPK
    nsv4832349copy number variation1nstd200human GRCh37 chr9: 127,994,292-128,017,622 , GRCh38.p12 chr9: 125,232,013-125,255,343 RABEPK, HSPA5, 1 more genes
    nsv4609539copy number variation1nstd183human GRCh37 chr9: 128,002,273-128,003,615 , GRCh38.p12 chr9: 125,239,994-125,241,336 HSPA5, HSPA5-DT
    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
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4183662copy number variation1nstd166human GRCh37.p13 chr9: 127,994,937-127,996,479 , GRCh38.p12 chr9: 125,232,658-125,234,200 RABEPK, HSPA5
    nsv4176245copy number variation1nstd166human GRCh37.p13 chr9: 128,001,000-128,008,000 , GRCh38.p12 chr9: 125,238,721-125,245,721 HSPA5-DT, HSPA5
    nsv3924370copy number variation1nstd102humanPathogenic NCBI36 chr9: 126,857,965-130,440,046 , GRCh38 chr9: 125,055,865-128,637,946 , GRCh37 chr9: 127,818,144-131,400,225 MVB12B, MIR4672, 97 more genes
    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
    nsv3922263copy number variation1nstd102humanPathogenic NCBI36 chr9: 124,897,698-128,495,943 , GRCh38 chr9: 123,095,598-126,693,843 , GRCh37 chr9: 125,857,877-129,456,122 OLFML2A, LHX2-AS1, 64 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
    nsv3920713copy number variation1nstd102humanPathogenic NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389 ABHD17B, LOC100533707, 2167 more genes
    nsv3919948copy number variation1nstd102humanPathogenic GRCh37 chr9: 125,554,937-141,018,984 , GRCh38 chr9: 122,792,658-138,124,532 , NCBI36 chr9: 124,594,758-140,138,805 LOC107987143, ATP6V1G1P3, 456 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center