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 356

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137090copy number variation1nstd102humanPathogenic GRCh37 chr2: 159,844,069-161,073,462 , GRCh38.p12 chr2: 158,987,557-160,216,951 CD302, LOC105373716, 16 more genes
    nsv7056410inversion1nstd229human GRCh38 chr2: 155,671,571-160,808,437 , GRCh37.p13 chr2: 156,528,083-161,664,948 LOC105373714, PKP4-AS1, 64 more genes
    nsv7038291inversion1nstd229human GRCh38 chr2: 160,124,761-160,124,806 , GRCh37.p13 chr2: 160,981,272-160,981,317 ITGB6
    nsv7038090inversion1nstd229human GRCh38 chr2: 152,079,952-160,943,714 , GRCh37.p13 chr2: 152,936,466-161,800,225 , ITGB6, 105 more genes
    nsv6695368copy number variation1nstd229human GRCh38 chr2: 160,099,084-160,140,352 , GRCh37.p13 chr2: 160,955,595-160,996,863 ITGB6
    nsv6694848copy number variation1nstd229human GRCh38 chr2: 160,192,360-160,194,794 , GRCh37.p13 chr2: 161,048,871-161,051,305 ITGB6
    nsv6692140copy number variation1nstd229human GRCh38 chr2: 160,160,956-160,168,116 , GRCh37.p13 chr2: 161,017,467-161,024,627 ITGB6
    nsv6690547copy number variation1nstd229human GRCh38 chr2: 160,174,491-160,174,702 , GRCh37.p13 chr2: 161,031,002-161,031,213 ITGB6
    nsv6687114copy number variation1nstd229human GRCh38 chr2: 160,110,946-160,218,330 , GRCh37.p13 chr2: 160,967,457-161,074,841 ITGB6
    nsv6686550copy number variation1nstd229human GRCh38 chr2: 160,141,401-160,166,300 , GRCh37.p13 chr2: 160,997,912-161,022,811 ITGB6
    nsv6685815copy number variation1nstd229human GRCh38 chr2: 159,859,239-160,223,059 , GRCh37.p13 chr2: 160,715,750-161,079,570 LY75, LOC105373717, 3 more genes
    nsv6683984copy number variation1nstd229human GRCh38 chr2: 160,134,210-160,178,918 , GRCh37.p13 chr2: 160,990,721-161,035,429 ITGB6
    nsv6683574copy number variation1nstd229human GRCh38 chr2: 160,131,088-160,158,438 , GRCh37.p13 chr2: 160,987,599-161,014,949 ITGB6
    nsv6682506copy number variation1nstd229human GRCh38 chr2: 160,194,295-160,194,934 , GRCh37.p13 chr2: 161,050,806-161,051,445 ITGB6
    nsv6678106copy number variation1nstd229human GRCh38 chr2: 159,978,101-160,112,800 , GRCh37.p13 chr2: 160,834,612-160,969,311 LOC105373717, ITGB6, 1 more genes
    nsv6636665copy number variation1nstd102humanUncertain significance GRCh37 chr2: 160,733,756-161,196,968 , GRCh38.p12 chr2: 159,877,245-160,340,457 ITGB6, LOC105373717, 5 more genes
    nsv6627717copy number variation1nstd224human GRCh37 chr2: 160,756,933-160,968,628 , GRCh38.p12 chr2: 159,900,422-160,112,117 ITGB6, PLA2R1, 3 more genes
    nsv6627357copy number variation1nstd224human GRCh37 chr2: 160,968,601-161,030,526 , GRCh38.p12 chr2: 160,112,090-160,174,015 ITGB6
    nsv6552172inversion1nstd223human GRCh38 chr2: 160,179,547-160,179,881 , GRCh37.p13 chr2: 161,036,058-161,036,392 ITGB6
    nsv6541715inversion1nstd223human GRCh38 chr2: 160,177,259-160,178,001 , GRCh37.p13 chr2: 161,033,770-161,034,512 ITGB6
    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