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 384

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095127copy number variation1nstd102humanUncertain significance GRCh37 chr16: 90,094,024-90,109,753 , GRCh38.p12 chr16: 90,027,616-90,043,345 URAHP, GAS8-AS1, 1 more genes
    nsv7094950copy number variation1nstd102humanUncertain significance GRCh37 chr16: 90,106,688-90,109,753 , GRCh38.p12 chr16: 90,040,280-90,043,345 GAS8, URAHP
    nsv7094949copy number variation1nstd102humanUncertain significance GRCh37 chr16: 90,094,024-90,099,352 , GRCh38.p12 chr16: 90,027,616-90,032,944 GAS8, GAS8-AS1
    nsv7094948copy number variation1nstd102humanUncertain significance GRCh37 chr16: 90,089,130-90,106,937 , GRCh38.p12 chr16: 90,022,722-90,040,529 URAHP, GAS8-AS1, 1 more genes
    nsv7094940copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,611,036-90,106,937 , GRCh38.p12 chr16: 89,544,628-90,040,529 SPATA2L, LINC02166, 25 more genes
    nsv7094699copy number variation2nstd102humanUncertain significance GRCh37 chr16: 87,636,753-90,109,753 , GRCh38.p12 chr16: 87,603,147-90,043,345 HSALR1, LOC105371412, 87 more genes
    nsv7093047copy number variation1nstd102humanUncertain significance GRCh37 chr16: 90,099,225-90,099,293 , GRCh38 chr16: 90,032,817-90,032,885 GAS8
    nsv7068471inversion1nstd229human GRCh38 chr16: 90,012,838-90,034,579 , GRCh37.p13 chr16: 90,079,246-90,100,987 GAS8, DBNDD1, 1 more genes
    nsv6995830copy number variation1nstd229human GRCh38 chr16: 90,036,665-90,060,759 , GRCh37.p13 chr16: 90,103,073-90,127,167 PRDM7, GAS8, 1 more genes
    nsv6994365copy number variation1nstd229human GRCh38 chr16: 90,002,953-90,080,293 , GRCh37.p13 chr16: 90,069,361-90,146,701 PRDM7, GAS8-AS1, 3 more genes
    nsv6992552copy number variation1nstd229human GRCh38 chr16: 90,014,227-90,040,253 , GRCh37.p13 chr16: 90,080,635-90,106,661 GAS8-AS1, GAS8, 2 more genes
    nsv6986741copy number variation1nstd229human GRCh38 chr16: 90,024,001-90,035,900 , GRCh37.p13 chr16: 90,090,409-90,102,308 GAS8-AS1, GAS8
    nsv6986303copy number variation1nstd229human GRCh38 chr16: 90,023,594-90,023,960 , GRCh37.p13 chr16: 90,090,002-90,090,368 GAS8
    nsv6982491copy number variation1nstd229human GRCh38 chr16: 90,021,014-90,043,596 , GRCh37.p13 chr16: 90,087,422-90,110,004 URAHP, GAS8-AS1, 1 more genes
    nsv6981628copy number variation1nstd229human GRCh38 chr16: 90,042,201-90,084,500 , GRCh37.p13 chr16: 90,108,609-90,150,908 GAS8, URAHP, 1 more genes
    nsv6979877copy number variation1nstd229human GRCh38 chr16: 89,999,531-90,055,074 , GRCh37.p13 chr16: 90,065,939-90,121,482 PRDM7, DBNDD1, 4 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6624189copy number variation1nstd224human GRCh37 chr16: 90,084,561-90,142,260 , GRCh38.p12 chr16: 90,018,153-90,075,852 GAS8, PRDM7, 3 more genes
    nsv6624031copy number variation1nstd224human GRCh37 chr16: 90,079,927-90,130,136 , GRCh38.p12 chr16: 90,013,519-90,063,728 GAS8-AS1, URAHP, 3 more genes
    nsv6623804copy number variation1nstd224human GRCh37 chr16: 90,079,534-90,130,152 , GRCh38.p12 chr16: 90,013,126-90,063,744 DBNDD1, GAS8, 3 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