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Items: 1 to 20 of 208

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099175copy number variation1nstd231human GRCh38.p12 chr1: 6,492,665-9,894,222 , GRCh37 chr1: 6,552,725-9,954,280 RERE, CA6, 70 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7058041inversion1nstd229human GRCh38 chr1: 1,845,355-9,534,096 , GRCh37.p13 chr1: 1,776,794-9,594,155 RPL37P9, TMEM52, 152 more genes
    nsv7057525inversion1nstd229human GRCh38 chr1: 7,829,944-15,116,659 , GRCh37.p13 chr1: 7,890,004-15,443,155 PEX14, RNU6-304P, 187 more genes
    nsv7054937inversion1nstd229human GRCh38 chr1: 8,856,621-8,936,364 , GRCh37.p13 chr1: 8,916,680-8,996,423 ENO1-AS1, RNU6-304P, 4 more genes
    nsv7054534inversion1nstd229human GRCh38 chr1: 2,972,403-10,562,308 , GRCh37.p13 chr1: 2,888,967-10,622,365 RN7SL731P, LOC105376682, 145 more genes
    nsv7052549inversion1nstd229human GRCh38 chr1: 8,322,830-13,737,741 , GRCh37.p13 chr1: 8,382,890-14,064,236 MIR4632, PLOD1, 166 more genes
    nsv7047983inversion1nstd229human GRCh38 chr1: 5,346,988-12,521,611 , GRCh37.p13 chr1: 5,407,048-12,581,655 THAP3, UBIAD1, 165 more genes
    nsv7046461inversion1nstd229human GRCh38 chr1: 5,352,168-12,521,473 , GRCh37.p13 chr1: 5,412,228-12,581,517 LINC02606, C1orf127, 165 more genes
    nsv7045918inversion1nstd229human GRCh38 chr1: 8,869,421-8,869,606 , GRCh37.p13 chr1: 8,929,480-8,929,665 ENO1
    nsv7044144inversion1nstd229human GRCh38 chr1: 6,762,728-10,175,549 , GRCh37.p13 chr1: 6,822,788-10,235,607 RPL7P11, LOC105376691, 68 more genes
    nsv6656735copy number variation1nstd229human GRCh38 chr1: 8,816,701-9,089,000 , GRCh37.p13 chr1: 8,876,760-9,149,059 ENO1, RNU6-304P, 10 more genes
    nsv6656603copy number variation1nstd229human GRCh38 chr1: 8,864,094-8,865,287 , GRCh37.p13 chr1: 8,924,153-8,925,346 MIR6728, ENO1
    nsv6656512copy number variation1nstd229human GRCh38 chr1: 8,851,543-9,119,084 , GRCh37.p13 chr1: 8,911,602-9,179,143 GPR157, RNU6-304P, 9 more genes
    nsv6655946copy number variation1nstd229human GRCh38 chr1: 8,871,953-8,876,825 , GRCh37.p13 chr1: 8,932,012-8,936,884 ENO1
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 more genes
    nsv6636785copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276 GPR157, MST1L, 313 more genes
    nsv6636244copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 8,473,813-9,852,687 , GRCh38.p12 chr1: 8,413,753-9,792,629 RERE, CA6, 33 more genes
    nsv6324723copy number variation1nstd223human GRCh38 chr1: 8,840,894-8,876,597 , GRCh37.p13 chr1: 8,900,953-8,936,656 MIR6728, ENO1
    nsv6321296copy number variation1nstd223human GRCh38 chr1: 8,877,801-8,879,500 , GRCh37.p13 chr1: 8,937,860-8,939,559 ENO1-AS1, ENO1
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