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Items: 1 to 20 of 378

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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
    nsv5673912copy number variation1nstd102humanPathogenic GRCh37 chrX: 21,958,943-22,208,619 , GRCh38.p12 chrX: 21,940,825-22,190,502 SMS, PHEX, 1 more genes
    nsv5422560copy number variation1nstd206human GRCh38 chrX: 21,968,051-21,968,103 , GRCh37.p13 chrX: 21,986,169-21,986,221 SMS
    nsv5375945translocation1nstd200human GRCh38 chrX: 21,961,099-21,961,099 , GRCh38 chrX: 21,961,021-21,961,021 , GRCh37.p13 chrX: 21,979,139-21,979,139 , GRCh37.p13 chrX: 21,979,217-21,979,217 SMS
    nsv5339870translocation1nstd200human GRCh37 chrX: 21,979,139-21,979,139 , GRCh37 chrX: 21,979,217-21,979,217 , GRCh38.p12 chrX: 21,961,099-21,961,099 , GRCh38.p12 chrX: 21,961,021-21,961,021 SMS
    nsv5190581mobile element insertion1nstd203human GRCh38 chrX: 21,938,776-21,938,797 , GRCh37.p13 chrX: 21,956,894-21,956,915 CYTH1P1, SMS
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4772538copy number variation1nstd200human GRCh37 chrX: 22,013,410-22,054,718 , GRCh38.p12 chrX: 21,995,292-22,036,600 SMS, PHEX
    nsv4728486copy number variation1nstd102humanPathogenic GRCh37 chrX: 219,609-55,466,476 , GRCh38.p12 chrX: 302,942-55,440,043 CDK16, WASF4P, 772 more genes
    nsv4682892copy number variation1nstd102humanPathogenic GRCh37 chrX: 21,990,015-22,292,386 , GRCh38.p12 chrX: 21,971,897-22,274,269 SMS, CBLL2, 3 more genes
    nsv4682193copy number variation1nstd102humanPathogenic GRCh37 chrX: 21,995,179-22,095,820 , GRCh38.p12 chrX: 21,977,061-22,077,702 PHEX, SMS
    nsv4674588copy number variation1nstd102humanPathogenic GRCh37 chrX: 539,722-55,509,385 , GRCh38.p12 chrX: 578,987-55,482,952 LOC392440, SSX4, 769 more genes
    nsv4674462copy number variation1nstd102humanUncertain significance GRCh37 chrX: 21,956,780-21,977,221 , GRCh38.p12 chrX: 21,938,662-21,959,103 CYTH1P1, SMS
    nsv4674458copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-34,753,512 , GRCh38.p12 chrX: 251,879-34,735,395 P2RY8, CA5BP1-CA5B, 344 more genes
    nsv4674282copy number variation1nstd102humanPathogenic GRCh37 chrX: 537,158-22,883,547 , GRCh38.p12 chrX: 576,423-22,865,430 NHS, EGFL6, 236 more genes
    nsv4454842copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,190,434-23,795,839 , GRCh38.p12 chrX: 2,272,393-23,777,722 MBTPS2, LOC101928389, 224 more genes
    nsv4452903copy number variation3nstd102humanUncertain significance GRCh37 chrX: 21,999,106-22,054,641 , GRCh38.p12 chrX: 21,980,988-22,036,523 PHEX, SMS
    nsv4452472copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-61,877,279 , GRCh38.p12 chrX: 251,879-62,657,809 MIR660, RNU6-1321P, 802 more genes
    nsv4452333copy number variation2nstd102humanPathogenic GRCh37 chrX: 13,962,918-22,148,232 , GRCh38.p12 chrX: 13,944,799-22,130,115 SETP15, RNU5F-7P, 96 more genes
    nsv4451942copy number variation1nstd102humanPathogenic GRCh37 chrX: 20,925,922-35,511,818 , GRCh38.p12 chrX: 20,907,804-35,493,701 LOC100420245, SNRPEP9, 117 more genes
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