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Items: 1 to 20 of 372

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5432989copy number variation1nstd206human GRCh38 chrX: 6,256,975-6,810,945 , GRCh37.p13 chrX: 6,175,016-6,728,986 RPS5P8, MIR4770, 2 more genes
    nsv5427518copy number variation1nstd206human GRCh38 chrX: 6,261,136-6,496,602 , GRCh37.p13 chrX: 6,179,177-6,414,643 RPS5P8, MIR4770
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4905140copy number variation1nstd200human GRCh38 chrX: 6,383,063-6,717,730 , GRCh37.p13 chrX: 6,301,104-6,635,771 VCX3A, MIR4770, 1 more genes
    nsv4905139copy number variation1nstd200human GRCh38 chrX: 6,379,673-6,609,106 , GRCh37.p13 chrX: 6,297,714-6,527,147 RPS5P8, MIR4770, 1 more genes
    nsv4905137copy number variation1nstd200human GRCh38 chrX: 6,248,098-6,482,738 , GRCh37.p13 chrX: 6,166,139-6,400,779 MIR4770, RPS5P8
    nsv4905135copy number variation1nstd200human GRCh38 chrX: 6,051,643-6,446,918 , GRCh37.p13 chrX: 5,969,684-6,364,959 RPS5P8, LOC105373156, 2 more genes
    nsv4769248copy number variation1nstd201human GRCh37 chrX: 168,546-21,870,371 , GRCh38.p12 chrX: 251,879-21,852,253 , AMELX, 248 more genes
    nsv4728746copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 3,185,613-6,333,434 , GRCh38.p12 chrX: 3,267,572-6,415,393 ASS1P4, PRKX, 24 more genes
    nsv4728721copy number variation1nstd102humanUncertain significance GRCh37 chrX: 5,975,976-6,659,291 , GRCh38.p12 chrX: 6,057,935-6,741,250 NLGN4X, MIR4770, 3 more genes
    nsv4728486copy number variation1nstd102humanPathogenic GRCh37 chrX: 219,609-55,466,476 , GRCh38.p12 chrX: 302,942-55,440,043 CDK16, WASF4P, 772 more genes
    nsv4680084copy number variation1nstd189human GRCh37.p13 chrX: 6,012,868-6,446,124 , GRCh38.p12 chrX: 6,094,827-6,528,083 NLGN4X, RPS5P8, 2 more genes
    nsv4679668copy number variation1nstd189human GRCh37.p13 chrX: 5,989,545-6,495,090 , GRCh38.p12 chrX: 6,071,504-6,577,049 VCX3A, NLGN4X, 3 more genes
    nsv4674815copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-17,502,124 , GRCh38.p12 chrX: 251,879-17,484,001 PTMAP14, LOC100132857, 189 more genes
    nsv4674792copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-6,449,753 , GRCh38.p12 chrX: 251,879-6,531,712 PPP2R3B, LOC652608, 68 more genes
    nsv4674615copy number variation1nstd102humanPathogenic GRCh37 chrX: 1,240,318-20,986,848 , GRCh38.p12 chrX: 1,140,165-20,968,730 RNA5SP499, GS1-600G8.3, 217 more genes
    nsv4674588copy number variation1nstd102humanPathogenic GRCh37 chrX: 539,722-55,509,385 , GRCh38.p12 chrX: 578,987-55,482,952 LOC392440, SSX4, 769 more genes
    nsv4674458copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-34,753,512 , GRCh38.p12 chrX: 251,879-34,735,395 P2RY8, CA5BP1-CA5B, 344 more genes
    nsv4674325copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-8,503,210 , GRCh38.p12 chrX: 251,879-8,535,169 PNPLA4, RPL14P5, 82 more genes
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