U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 25

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3877822copy number variation1nstd102humanBenign GRCh37 chr2: 170,368,695-170,517,503 , GRCh38.p12 chr2: 169,512,185-169,660,993 FASTKD1, LOC100421474, 3 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv4451512copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,329,586-192,756,373 , GRCh38.p12 chr2: 166,473,076-191,891,647 LINC01117, LOC107985958, 339 more genes
    nsv4768307copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890 RBM45, LOC102724194, 258 more genes
    nsv3904056copy number variation1nstd102humanPathogenic GRCh37 chr2: 164,821,892-183,059,789 , NCBI36 chr2: 164,530,138-182,768,034 , GRCh38 chr2: 163,965,382-182,195,062 PRKRA, STK39, 256 more genes
    nsv6315160copy number variation1nstd102humanPathogenic GRCh37 chr2: 160,347,642-174,075,851 , GRCh38.p12 chr2: 159,491,131-173,211,123 EIF3EP3, FAP, 158 more genes
    nsv3909452copy number variation1nstd102humanPathogenic GRCh37 chr2: 165,706,627-176,423,918 , GRCh38 chr2: 164,850,117-175,559,190 , NCBI36 chr2: 165,414,873-176,132,164 LOC107985959, TTC21B, 141 more genes
    nsv3914220copy number variation1nstd102humanPathogenic NCBI36 chr2: 166,992,294-175,094,656 , GRCh37.p13 chr2: 167,284,048-175,386,410 , GRCh38.p12 chr2: 166,427,538-174,521,682 GPR155-DT, DAP3P2, 111 more genes
    nsv3903934copy number variation1nstd102humanPathogenic GRCh37 chr2: 164,922,548-172,962,614 , NCBI36 chr2: 164,630,794-172,670,860 , GRCh38 chr2: 164,066,038-172,097,886 LOC105373739, RNA5SP110, 95 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 IGKV2OR2-10, LOC105374848, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 RNU6-674P, KANSL3, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 MTND2P22, LOC112268410, 3724 more genes
    nsv4674383copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464 SNORA41, LOC101929633, 663 more genes
    nsv3876037copy number variation1nstd102humanPathogenic GRCh37 chr2: 169,829,974-215,521,436 , GRCh38.p12 chr2: 168,973,464-214,656,712 LINC01953, CTLA4, 632 more genes
    nsv3875392copy number variation1nstd102humanPathogenic GRCh37 chr2: 152,409,978-179,325,736 , GRCh38.p12 chr2: 151,553,464-178,461,009 MIR10B, SCN7A, 359 more genes
    nsv3874278copy number variation1nstd102humanPathogenic GRCh37 chr2: 156,489,430-182,921,298 , GRCh38.p12 chr2: 155,632,918-182,056,571 LOC107985957, LOC101927073, 358 more genes
    nsv3893853copy number variation1nstd102humanPathogenic GRCh38 chr2: 154,294,042-175,989,372 , GRCh37 chr2: 155,150,555-176,854,100 , NCBI36 chr2: 154,858,801-176,562,346 SCN7A, HEBP2P1, 275 more genes
    nsv1398397copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 167,996,718-170,671,886 , GRCh38.p12 chr2: 167,140,208-169,815,376 LRP2, SSB, 36 more genes
    nsv3880118copy number variation1nstd102humanBenign GRCh37 chr2: 170,343,083-170,680,879 , GRCh38.p12 chr2: 169,486,573-169,824,369 CYB5AP2, PTCHD3P2, 13 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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