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Items: 1 to 20 of 288

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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
    nsv5882824copy number variation1nstd209human GRCh38 chrX: 44,722,720-48,672,672 , GRCh37.p13 chrX: 44,581,966-47,619,970 ZNF674-AS1, CDK16, 115 more genes
    nsv5873682copy number variation1nstd209human GRCh38 chrX: 41,560,623-47,265,899 , GRCh37.p13 chrX: 41,419,876-47,125,298 , CTNNBL1P1, 80 more genes
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5556729sequence alteration1nstd206human GRCh37.p13 chrX|NW_004166866.1: 111,970-469,972 , GRCh38 chrX: 46,862,409-47,356,182 , GRCh37.p13 chrX: 46,721,844-47,079,810 USP11, RGN, 16 more genes
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5381699copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,696,536-47,436,910 , GRCh38.p12 chrX: 46,837,101-47,577,511 LINC01560, LOC105373194, 25 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
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4728606copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,942,052-47,379,255 , GRCh38.p12 chrX: 47,082,653-47,519,856 LOC100419232, ZNF41, 20 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
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 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
    nsv4578278inversion1nstd102humanLikely pathogenic GRCh37 chrX: 32,196,272-75,245,806 , GRCh38.p12 chrX: 32,178,155-76,025,971 ABCB7, ACTG1P10, 704 more genes
    nsv4452472copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-61,877,279 , GRCh38.p12 chrX: 251,879-62,657,809 MIR660, RNU6-1321P, 802 more genes
    nsv4450820copy number variation1nstd102humanPathogenic GRCh37 chrX: 40,572,613-92,796,528 , GRCh38.p12 chrX: 40,713,361-93,541,529 HNRNPA1P25, MPV17L2P1, 755 more genes
    nsv4436319copy number variation1nstd102humanPathogenic GRCh37 chrX: 1-47,140,860 , GRCh38.p12 chrX: 10,001-47,281,461 RNU6-266P, MID1IP1, 515 more genes
    nsv4436196copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,814-50,519,984 , GRCh38.p12 chrX: 10,814-50,776,984 CTPS2, CLTRN, 653 more genes
    nsv4380296copy number variation3nstd173human GRCh37 chrX: 168,547-155,233,756 , GRCh38.p12 chrX: 251,880-156,004,091 , RPL31P63, 2192 more genes
    nsv4367211copy number variation1nstd173human GRCh37 chrX: 168,547-155,233,756 , GRCh38.p12 chrX: 251,880-156,004,091 , MIR421, 2192 more genes
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