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 93

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6837345copy number variation1nstd229human GRCh38 chr7: 45,250,752-45,259,454 , GRCh37.p13 chr7: 45,290,351-45,299,053 LOC107986736
    nsv6837220copy number variation1nstd229human GRCh38 chr7: 45,252,999-45,508,609 , GRCh37.p13 chr7: 45,292,598-45,548,208 LOC100419775, ELK1P1, 1 more genes
    nsv6821159copy number variation1nstd229human GRCh38 chr7: 45,244,145-45,261,608 , GRCh37.p13 chr7: 45,283,744-45,301,207 LOC107986736
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6574607inversion1nstd223human GRCh38 chr7: 35,958,610-45,735,691 , GRCh37.p13 chr7: 35,998,220-45,775,290 RPS17P13, LOC105375252, 182 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313816copy number variation1nstd102humanUncertain significance GRCh37 chr7: 44,765,589-45,364,793 , GRCh38.p12 chr7: 44,725,990-45,325,194 LOC100419775, H2AZ2-DT, 20 more genes
    nsv6313509copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,778,439-50,228,656 , GRCh38.p12 chr7: 40,738,840-50,189,060 LINC01447, ABCA13, 142 more genes
    nsv6136995copy number variation1nstd213human GRCh37 chr7: 39,040,000-48,190,001 , GRCh38.p12 chr7: 39,000,400-48,150,404 ADCY1, AEBP1, 161 more genes
    nsv6135995copy number variation1nstd213human GRCh37 chr7: 44,480,000-45,360,001 , GRCh38.p12 chr7: 44,440,401-45,320,402 PURB, NPC1L1, 28 more genes
    nsv6135992copy number variation1nstd213human GRCh37 chr7: 39,290,000-48,200,001 , GRCh38.p12 chr7: 39,250,401-48,160,404 PSMA2, RALA, 160 more genes
    nsv5556950sequence alteration1nstd206human GRCh38 chr7: 44,712,903-47,388,095 , GRCh37.p13 chr7: 44,752,502-47,427,692 , ADCY1, 51 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5493221copy number variation1nstd206human GRCh38 chr7: 45,247,968-45,271,109 , GRCh37.p13 chr7: 45,287,567-45,310,708 LOC107986736
    nsv5492849copy number variation1nstd206human GRCh38 chr7: 45,256,302-45,256,398 , GRCh37.p13 chr7: 45,295,901-45,295,997 LOC107986736
    nsv5381787copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,341,583-50,171,623 , GRCh38.p12 chr7: 43,301,984-50,132,027 OGDH, LOC112267918, 110 more genes
    nsv5381783copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969 ELK1P1, URGCP, 121 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956469copy number variation1nstd200human GRCh38 chr7: 45,258,701-45,277,390 , GRCh37.p13 chr7: 45,298,300-45,316,989 LOC107986736
    nsv4956468copy number variation1nstd200human GRCh38 chr7: 45,250,752-45,259,451 , GRCh37.p13 chr7: 45,290,351-45,299,050 LOC107986736
    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