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 302

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5727450mobile element insertion2nstd211human GRCh38 chr11: 126,222,515-126,222,515 , GRCh37.p13 chr11: 126,092,410-126,092,410 FAM118B
    nsv5706595mobile element insertion1nstd211human GRCh38 chr11: 126,214,527-126,214,527 , GRCh37.p13 chr11: 126,084,422-126,084,422 RNU4-86P, FAM118B
    nsv5702162mobile element insertion1nstd211human GRCh38 chr11: 126,214,490-126,214,490 , GRCh37.p13 chr11: 126,084,385-126,084,385 RNU4-86P, FAM118B
    nsv5652592insertion4nstd207human GRCh38 chr11: 126,226,100-126,226,100 , GRCh37.p13 chr11: 126,095,995-126,095,995 FAM118B
    nsv5648661insertion1nstd207human GRCh38 chr11: 126,226,382-126,226,382 , GRCh37.p13 chr11: 126,096,277-126,096,277 FAM118B
    nsv5648631insertion1nstd207human GRCh38 chr11: 126,226,429-126,226,429 , GRCh37.p13 chr11: 126,096,324-126,096,324 FAM118B
    nsv5559433mobile element insertion1nstd206human GRCh38 chr11: 126,222,515-126,222,566 , GRCh37.p13 chr11: 126,092,410-126,092,461 FAM118B
    nsv5507858copy number variation1nstd206human GRCh38 chr11: 126,235,685-126,239,621 , GRCh37.p13 chr11: 126,105,580-126,109,516 FAM118B
    nsv5134106mobile element insertion1nstd203human GRCh38 chr11: 126,219,389-126,219,389 , GRCh37.p13 chr11: 126,089,284-126,089,284 FAM118B
    nsv5132019mobile element insertion1nstd203human GRCh38 chr11: 126,214,490-126,214,490 , GRCh37.p13 chr11: 126,084,385-126,084,385 RNU4-86P, FAM118B
    nsv5121855mobile element insertion1nstd203human GRCh38 chr11: 126,219,349-126,219,389 , GRCh37.p13 chr11: 126,089,244-126,089,284 FAM118B
    nsv4974116copy number variation1nstd200human GRCh38 chr11: 126,245,060-126,254,735 , GRCh37.p13 chr11: 126,114,955-126,124,630 SRPRA, RN7SL351P, 1 more genes
    nsv4841097copy number variation1nstd200human GRCh37 chr11: 126,097,808-126,099,472 , GRCh38.p12 chr11: 126,227,913-126,229,577 FAM118B
    nsv4758209insertion1nstd199human GRCh37 chr11: 126,095,958-126,095,958 , GRCh38.p12 chr11: 126,226,063-126,226,063 FAM118B
    nsv4745972copy number variation1nstd199human GRCh37 chr11: 126,095,958-126,096,367 , GRCh38.p12 chr11: 126,226,063-126,226,472 FAM118B
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4732620copy number variation1nstd199human GRCh37 chr11: 126,120,074-126,120,153 , GRCh38.p12 chr11: 126,250,179-126,250,258 FAM118B
    nsv4728891copy number variation1nstd102humanPathogenic GRCh37 chr11: 125,785,487-134,938,470 , GRCh38.p12 chr11: 125,915,592-135,068,576 ARHGAP32, NAP1L1P1, 125 more genes
    nsv4675832copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576 MIR8052, BLID, 275 more genes
    nsv4675674copy number variation1nstd102humanPathogenic GRCh37 chr11: 124,232,608-134,938,470 , GRCh38.p12 chr11: 124,362,712-135,068,576 FAM118B, PUS3, 184 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