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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5912321copy number variation1nstd209human GRCh38 chr11: 126,291,399-126,292,450 , GRCh37.p13 chr11: 126,161,294-126,162,345 TIRAP, TIRAP-AS1
    nsv5908823copy number variation1nstd209human GRCh38 chr11: 126,290,630-126,292,839 , GRCh37.p13 chr11: 126,160,525-126,162,734 TIRAP-AS1, TIRAP
    nsv5865883copy number variation1nstd209human GRCh38 chr11: 126,291,339-126,292,847 , GRCh37.p13 chr11: 126,161,234-126,162,742 TIRAP-AS1, TIRAP
    nsv5852698copy number variation1nstd209human GRCh38 chr11: 126,291,338-126,292,547 , GRCh37.p13 chr11: 126,161,233-126,162,442 TIRAP, TIRAP-AS1
    nsv5510057copy number variation1nstd206human GRCh38 chr11: 126,291,397-126,292,540 , GRCh37.p13 chr11: 126,161,292-126,162,435 TIRAP, TIRAP-AS1
    nsv5505663copy number variation1nstd206human GRCh38 chr11: 126,290,633-126,292,840 , GRCh37.p13 chr11: 126,160,528-126,162,735 TIRAP-AS1, TIRAP
    nsv5310267copy number variation1nstd204human GRCh37.p13 chr11: 126,161,332-126,162,368 , GRCh38.p13 chr11: 126,291,437-126,292,473 TIRAP-AS1, TIRAP
    nsv5279990copy number variation1nstd204human GRCh38.p13 chr11: 126,298,201-126,307,200 , GRCh37.p13 chr11: 126,168,096-126,177,095 TIRAP-AS1, DCPS
    nsv5125843mobile element insertion1nstd203human GRCh38 chr11: 126,297,109-126,297,123 , GRCh37.p13 chr11: 126,167,004-126,167,018 TIRAP-AS1
    nsv4831259copy number variation1nstd200human GRCh37 chr11: 126,165,184-126,165,984 , GRCh38.p12 chr11: 126,295,289-126,296,089 TIRAP, TIRAP-AS1
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    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
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4673961copy number variation1nstd102humanPathogenic GRCh37 chr11: 124,226,940-134,944,477 , GRCh38.p12 chr11: 124,357,044-135,074,583 OR8A2P, LOC101929473, 186 more genes
    nsv4673426copy number variation1nstd186human GRCh37 chr11: 126,160,525-126,162,735 , GRCh38.p12 chr11: 126,290,630-126,292,840 TIRAP-AS1, TIRAP
    nsv4666789copy number variation1nstd186human GRCh37 chr11: 126,161,335-126,162,400 , GRCh38.p12 chr11: 126,291,440-126,292,505 TIRAP, TIRAP-AS1
    nsv4615609copy number variation1nstd183human GRCh37 chr11: 126,160,525-126,162,735 , GRCh38.p12 chr11: 126,290,630-126,292,840 TIRAP, TIRAP-AS1
    nsv4614937copy number variation1nstd183human GRCh37 chr11: 126,161,335-126,162,400 , GRCh38.p12 chr11: 126,291,440-126,292,505 TIRAP, TIRAP-AS1
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