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 262

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7056199inversion1nstd229human GRCh38 chr2: 216,065,211-216,070,064 , GRCh37.p13 chr2: 216,929,934-216,934,787 PECR
    nsv7044853inversion1nstd229human GRCh38 chr2: 216,007,188-216,178,929 , GRCh37.p13 chr2: 216,871,911-217,043,652 TMEM169, LOC100421349, 4 more genes
    nsv6693271copy number variation1nstd229human GRCh38 chr2: 216,043,451-216,047,864 , GRCh37.p13 chr2: 216,908,174-216,912,587 PECR
    nsv6691426copy number variation1nstd229human GRCh38 chr2: 215,046,725-216,125,546 , GRCh37.p13 chr2: 215,911,449-216,990,269 LOC107985982, ATIC, 12 more genes
    nsv6688095copy number variation1nstd229human GRCh38 chr2: 216,040,701-216,045,100 , GRCh37.p13 chr2: 216,905,424-216,909,823 PECR
    nsv6687951copy number variation1nstd229human GRCh38 chr2: 216,066,537-216,066,603 , GRCh37.p13 chr2: 216,931,260-216,931,326 PECR
    nsv6684728copy number variation1nstd229human GRCh38 chr2: 216,055,507-216,058,728 , GRCh37.p13 chr2: 216,920,230-216,923,451 PECR
    nsv6678758copy number variation1nstd229human GRCh38 chr2: 216,047,171-216,057,881 , GRCh37.p13 chr2: 216,911,894-216,922,604 PECR
    nsv6554921inversion1nstd223human GRCh38 chr2: 216,053,985-216,054,407 , GRCh37.p13 chr2: 216,918,708-216,919,130 PECR
    nsv6554078inversion1nstd223human GRCh38 chr2: 216,030,583-216,031,172 , GRCh37.p13 chr2: 216,895,306-216,895,895 PECR, MREG
    nsv6549272inversion1nstd223human GRCh38 chr2: 216,063,337-216,063,843 , GRCh37.p13 chr2: 216,928,060-216,928,566 PECR
    nsv6548841inversion1nstd223human GRCh38 chr2: 216,077,146-216,079,532 , GRCh37.p13 chr2: 216,941,869-216,944,255 PECR
    nsv6548646inversion1nstd223human GRCh38 chr2: 216,046,334-216,046,870 , GRCh37.p13 chr2: 216,911,057-216,911,593 PECR
    nsv6545450inversion1nstd223human GRCh38 chr2: 216,030,614-216,031,398 , GRCh37.p13 chr2: 216,895,337-216,896,121 PECR, MREG
    nsv6544371inversion1nstd223human GRCh38 chr2: 216,076,910-216,077,363 , GRCh37.p13 chr2: 216,941,633-216,942,086 PECR
    nsv6540598inversion1nstd223human GRCh38 chr2: 216,067,653-216,068,182 , GRCh37.p13 chr2: 216,932,376-216,932,905 PECR
    nsv6353389copy number variation1nstd223human GRCh38 chr2: 216,055,501-216,057,700 , GRCh37.p13 chr2: 216,920,224-216,922,423 PECR
    nsv6348450copy number variation1nstd223human GRCh38 chr2: 215,046,725-216,125,546 , GRCh37.p13 chr2: 215,911,449-216,990,269 LOC107985982, LOC102724849, 12 more genes
    nsv6338935copy number variation1nstd223human GRCh38 chr2: 216,040,690-216,045,079 , GRCh37.p13 chr2: 216,905,413-216,909,802 PECR
    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