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Items: 1 to 20 of 594

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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
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5564472copy number variation1nstd102humanPathogenic GRCh37 chrY: 10,701-5,080,415 , GRCh38.p12 chrY: 10,701-5,212,374 AGPAT5P1, NAP1L1P2, 58 more genes
    nsv5432327copy number variation1nstd206human GRCh38 chrX: 10,000-2,781,000 , GRCh37.p13 chrX: 60,001-2,699,041 , IL3RA, 40 more genes
    nsv5431814copy number variation1nstd206human GRCh38 chrX: 2,531,036-2,924,507 , GRCh37.p13 chrX: 2,449,077-2,842,548 ARSD, CD99, 7 more genes
    nsv5415892copy number variation1nstd206human GRCh38 chrX: 2,527,829-2,636,084 , GRCh37.p13 chrX: 2,445,870-2,554,125 LINC03112, MIR6089, 2 more genes
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4905107copy number variation1nstd200human GRCh38 chrX: 2,501,273-2,671,970 , GRCh37.p13 chrX: 2,419,314-2,590,011 DHRSX, CD99P1, 4 more genes
    nsv4905106copy number variation1nstd200human GRCh38 chrX: 2,472,407-3,562,929 , GRCh37.p13 chrX: 2,390,448-3,480,970 MXRA5, LINC01546, 17 more genes
    nsv4772447copy number variation1nstd200human GRCh37 chrX: 2,348,836-2,570,760 , GRCh38.p12 chrX: 2,430,795-2,652,719 CD99P1, LINC00102, 4 more genes
    nsv4769315copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-4,857,212 , GRCh38.p12 chrX: 10,001-4,939,171 AKAP17A, RPS27AP20, 58 more genes
    nsv4769248copy number variation1nstd201human GRCh37 chrX: 168,546-21,870,371 , GRCh38.p12 chrX: 251,879-21,852,253 , AMELX, 248 more genes
    nsv4728687copy number variation1nstd102humanUncertain significance GRCh37 chrY: 1,873,925-2,800,880 , GRCh38.p12 chrY: 1,805,032-2,932,839 HSFY3P, NAP1L1P2, 14 more genes
    nsv4728529copy number variation1nstd102humanLikely benign GRCh37 chrX: 2,203,840-2,552,145 , GRCh38.p12 chrX: 2,285,799-2,634,104 ZBED1, LINC00102, 4 more genes
    nsv4728502copy number variation1nstd102humanUncertain significance GRCh37 chrX: 2,428,084-3,118,627 , GRCh38.p12 chrX: 2,510,043-3,200,586 CD99, ARSD, 11 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
    nsv4728341copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,227,053-2,571,725 , GRCh38.p12 chrX: 1,126,900-2,653,684 IL3RA, LINC03112, 22 more genes
    nsv4728201copy number variation1nstd102humanLikely benign GRCh37 chrX: 1,922,918-2,689,886 , GRCh38.p12 chrX: 1,804,025-2,771,845 DHRSX, LINC03112, 7 more genes
    nsv4728149copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,688,006-2,571,725 , GRCh38.p12 chrX: 1,569,113-2,653,684 LINC02968, LINC00102, 9 more genes
    nsv4728135copy number variation1nstd102humanUncertain significance GRCh37 chrX: 2,422,650-2,965,166 , GRCh38.p12 chrX: 2,504,609-3,047,125 XG, MIR6089, 10 more genes
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