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Items: 1 to 20 of 16733

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6130248mobile element insertion1nstd186human GRCh37 chr18: 28,732,918-28,732,960 , GRCh38.p12 chr18: 31,152,955-31,152,997 DSC1, DSCAS
    nsv6130159insertion1nstd186human GRCh37 chr17: 38,975,146-38,975,154 , GRCh38.p12 chr17: 40,818,894-40,818,902 KRT10, KRT10-AS1
    nsv6129381insertion1nstd186human GRCh37 chr18: 28,730,340-28,730,360 , GRCh38.p12 chr18: 31,150,377-31,150,397 DSC1, DSCAS
    nsv6127563copy number variation1nstd186human GRCh37 chr18: 28,677,393-28,677,902 , GRCh38.p12 chr18: 31,097,430-31,097,939 DSC2
    nsv6126674copy number variation1nstd186human GRCh37 chr17: 39,383,977-39,395,052 , GRCh38.p12 chr17: 41,227,725-41,238,800 , GRCh38.p12 chr17|NW_003871092.1: 58,054-69,063 KRTAP9-2, KRTAP9-3, 1 more genes
    nsv6125938copy number variation1nstd186human GRCh37 chr17: 39,506,842-39,525,741 , GRCh38.p12 chr17: 41,350,590-41,369,489 , GRCh38.p12 chr17|NW_003315953.2: 70,772-89,671 KRT33A, KRT33B, 1 more genes
    nsv6124019copy number variation1nstd186human GRCh37 chr17: 39,197,506-39,197,593 , GRCh38.p12 chr17: 41,041,254-41,041,341 , GRCh38.p12 chr17|NW_003871091.1: 190,647-190,734 KRTAP1-1
    nsv6123458copy number variation1nstd186human GRCh37 chr17: 39,203,202-39,211,742 , GRCh38.p12 chr17: 41,046,950-41,055,490 , GRCh38.p12 chr17|NW_003871091.1: 196,343-204,988 KRTAP2-2, KRTAP2-1
    nsv6122902copy number variation1nstd186human GRCh37 chr11: 390,478-390,903 , GRCh38.p12 chr11: 390,478-390,903 PKP3
    nsv6120171copy number variation1nstd186human GRCh37 chr1: 152,276,679-152,281,567 , GRCh38.p12 chr1: 152,304,203-152,309,091 FLG
    nsv6116893mobile element insertion1nstd186human GRCh37 chr1: 152,748,428-152,748,479 , GRCh38.p12 chr1: 152,775,952-152,776,003 LCE1F
    nsv6114033mobile element insertion1nstd186human GRCh37 chr12: 52,685,503-52,685,554 , GRCh38.p12 chr12: 52,291,719-52,291,770 KRT81, KRT86
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv6112726copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478 SIMALR, MTFR2, 99 more genes
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5980049insertion1nstd209human GRCh38 chr16: 4,889,231-4,889,231 , GRCh37.p13 chr16: 4,939,232-4,939,232 PPL
    nsv5978189inversion1nstd209human GRCh38 chr21: 44,550,659-44,628,117 , GRCh37.p13 chr21: 45,970,542-46,048,034 , GRCh37.p13 chr21|NW_004775435.1: 53,982-131,440 TSPEAR, KRTAP10-4, 7 more genes
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