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 227

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112763copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,145-7,730,395 , GRCh38.p12 chr12: 79,979-7,577,799 GALNT8, LINC02371, 197 more genes
    nsv5917209copy number variation1nstd209human GRCh38 chr12: 84,357-186,059 , GRCh37.p13 chr12|NW_003571048.1: 74,357-163,298 , GRCh37.p13 chr12: 193,523-282,464 IQSEC3-AS2, IQSEC3-AS1, 2 more genes
    nsv5861704copy number variation1nstd209human GRCh38 chr12: 104,606-108,989 , GRCh37.p13 chr12|NW_003571048.1: 94,606-98,989 , GRCh37.p13 chr12: 213,772-218,155 IQSEC3, IQSEC3-AS2
    nsv5860610copy number variation1nstd209human GRCh38 chr12: 109,490-121,546 , GRCh37.p13 chr12|NW_003571048.1: 99,490-111,546 , GRCh37.p13 chr12: 218,656-230,712 IQSEC3, IQSEC3-AS2
    nsv5854771copy number variation1nstd209human GRCh38 chr12: 106,506-110,089 , GRCh37.p13 chr12|NW_003571048.1: 96,506-100,089 , GRCh37.p13 chr12: 215,672-219,255 IQSEC3, IQSEC3-AS2
    nsv5851767copy number variation1nstd209human GRCh38 chr12: 108,490-110,689 , GRCh37.p13 chr12|NW_003571048.1: 98,490-100,689 , GRCh37.p13 chr12: 217,656-219,855 IQSEC3, IQSEC3-AS2
    nsv5708544mobile element insertion1nstd211human GRCh38 chr12: 109,154-109,154 , GRCh37.p13 chr12: 218,320-218,320 , GRCh37.p13 chr12|NW_003571048.1: 99,154-99,154 IQSEC3, IQSEC3-AS2
    nsv5511849copy number variation1nstd206human GRCh38 chr12: 38,500-163,000 , GRCh37.p13 chr12|NW_003571048.1: 28,500-153,000 , GRCh37.p13 chr12: 154,906-272,166 IQSEC3, LOC574538, 3 more genes
    nsv5415401mobile element insertion1nstd206human GRCh38 chr12: 109,154-109,205 , GRCh37.p13 chr12|NW_003571048.1: 99,154-99,205 , GRCh37.p13 chr12: 218,320-218,371 IQSEC3-AS2, IQSEC3
    nsv5373939translocation1nstd200human GRCh38 chr12: 109,573-109,573 , GRCh38 chr12: 130,409-130,409 , GRCh37.p13 chr12: 239,575-239,575 , GRCh37.p13 chr12|NW_003571048.1: 120,409-120,409 , GRCh37.p13 chr12|NW_003571048.1: 99,573-99,573 , GRCh37.p13 chr12: 218,739-218,739 IQSEC3-AS2, IQSEC3
    nsv5267828copy number variation1nstd204human GRCh38.p13 chr12: 109,190-110,289 , GRCh37.p13 chr12|NW_003571048.1: 99,190-100,289 , GRCh37.p13 chr12: 218,356-219,455 IQSEC3, IQSEC3-AS2
    nsv4974204copy number variation1nstd200human GRCh38 chr12: 80,857-438,294 , GRCh37.p13 chr12: 282,465-547,460 LOC105369594, SLC6A12, 9 more genes
    nsv4829660copy number variation1nstd200human GRCh37 chr12: 190,023-547,460 , GRCh38.p12 chr12: 80,857-438,294 SLC6A12-AS1, LOC105369594, 9 more genes
    nsv4765521inversion1nstd199human GRCh37 chr12: 164,697-2,866,263 , GRCh38.p12 chr12: 55,531-2,757,097 , CACNA1C, 51 more genes
    nsv4729176copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,242-4,683,495 , GRCh38.p12 chr12: 82,076-4,574,329 RPL18P9, CACNA1C, 92 more genes
    nsv4684316copy number variation1nstd102humanBenign NCBI36 chr12: 16,001-100,682 , GRCh37 chr12: 70,794-230,421 , GRCh38 chr12|NW_003571049.1: 33,647-115,270 IQSEC3-AS2, IQSEC3
    nsv4680514copy number variation1nstd189human GRCh37.p13 chr12: 1-807,399 , GRCh38.p12 chr12: 45,740-698,233 NINJ2, KDM5A, 16 more genes
    nsv4674893copy number variation1nstd102humanUncertain significance GRCh37 chr12: 173,786-825,782 , GRCh38.p12 chr12: 64,620-716,616 SLC6A12-AS1, RNU7-103P, 16 more genes
    nsv4606107copy number variation1nstd183human GRCh37 chr12: 150,442-373,724 , GRCh38.p12 chr12: 45,740-264,558 , GRCh38.p12 chr12|NW_003571049.1: 33,495-167,313 SLC6A12, SLC6A13, 6 more genes
    nsv4605246copy number variation1nstd183human GRCh37 chr12: 178,837-216,039 , GRCh38.p12 chr12|NW_003571049.1: 63,686-100,888 , GRCh38.p12 chr12: 69,671-106,873 IQSEC3-AS2, IQSEC3
    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