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 932

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7057531inversion1nstd229human GRCh38 chr3: 100,063,314-100,076,393 , GRCh37.p13 chr3: 99,782,158-99,795,237 FILIP1L, CMSS1
    nsv7055012inversion1nstd229human GRCh38 chr3: 99,875,353-99,881,500 , GRCh37.p13 chr3: 99,594,197-99,600,344 CMSS1, FILIP1L
    nsv7054009inversion1nstd229human GRCh38 chr3: 99,853,615-99,862,119 , GRCh37.p13 chr3: 99,572,459-99,580,963 FILIP1L, CMSS1
    nsv7053627inversion1nstd229human GRCh38 chr3: 99,989,434-100,110,476 , GRCh37.p13 chr3: 99,708,278-99,829,320 CMSS1, FILIP1L, 1 more genes
    nsv7052135inversion1nstd229human GRCh38 chr3: 100,117,132-100,119,572 , GRCh37.p13 chr3: 99,835,976-99,838,416 CMSS1
    nsv7050830inversion1nstd229human GRCh38 chr3: 100,119,815-100,141,519 , GRCh37.p13 chr3: 99,838,659-99,860,363 CMSS1
    nsv7048802inversion1nstd229human GRCh38 chr3: 99,928,651-99,928,726 , GRCh37.p13 chr3: 99,647,495-99,647,570 FILIP1L, CMSS1
    nsv7046832inversion1nstd229human GRCh38 chr3: 99,875,218-99,885,524 , GRCh37.p13 chr3: 99,594,062-99,604,368 FILIP1L, CMSS1
    nsv7046696inversion1nstd229human GRCh38 chr3: 100,069,563-100,076,589 , GRCh37.p13 chr3: 99,788,407-99,795,433 FILIP1L, CMSS1
    nsv7041946inversion1nstd229human GRCh38 chr3: 99,850,345-99,850,447 , GRCh37.p13 chr3: 99,569,189-99,569,291 CMSS1, FILIP1L
    nsv6717606copy number variation1nstd229human GRCh38 chr3: 99,985,911-99,985,936 , GRCh37.p13 chr3: 99,704,755-99,704,780 CMSS1, FILIP1L
    nsv6716562copy number variation1nstd229human GRCh38 chr3: 100,066,519-100,066,826 , GRCh37.p13 chr3: 99,785,363-99,785,670 CMSS1, FILIP1L
    nsv6716510copy number variation1nstd229human GRCh38 chr3: 100,146,901-100,159,100 , GRCh37.p13 chr3: 99,865,745-99,877,944 LOC105374009, CMSS1
    nsv6716238copy number variation1nstd229human GRCh38 chr3: 100,114,666-100,118,427 , GRCh37.p13 chr3: 99,833,510-99,837,271 CMSS1, FILIP1L
    nsv6715900copy number variation1nstd229human GRCh38 chr3: 99,870,613-99,923,562 , GRCh37.p13 chr3: 99,589,457-99,642,406 FILIP1L, CMSS1
    nsv6715713copy number variation1nstd229human GRCh38 chr3: 100,079,362-100,079,509 , GRCh37.p13 chr3: 99,798,206-99,798,353 FILIP1L, CMSS1
    nsv6715374copy number variation1nstd229human GRCh38 chr3: 100,177,553-100,190,370 , GRCh37.p13 chr3: 99,896,397-99,909,214 CMSS1, TMEM30CP
    nsv6714676copy number variation1nstd229human GRCh38 chr3: 99,964,900-99,968,157 , GRCh37.p13 chr3: 99,683,744-99,687,001 CMSS1, FILIP1L
    nsv6714133copy number variation1nstd229human GRCh38 chr3: 100,013,157-100,021,319 , GRCh37.p13 chr3: 99,732,001-99,740,163 CMSS1, LOC105374010, 1 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