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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099238copy number variation1nstd231human GRCh38.p12 chr1: 158,547,193-159,184,138 , GRCh37 chr1: 158,516,983-159,153,928 IFI16, MNDA, 23 more genes
    nsv7041047inversion1nstd229human GRCh38 chr1: 154,596,558-159,585,927 , GRCh37.p13 chr1: 154,569,034-159,555,717 ADAR, SNORA80E, 204 more genes
    nsv6642951copy number variation1nstd229human GRCh38 chr1: 158,591,310-158,638,113 , GRCh37.p13 chr1: 158,561,100-158,607,903 SPTA1, OR10Z1
    nsv6642598copy number variation1nstd229human GRCh38 chr1: 158,519,625-158,923,791 , GRCh37.p13 chr1: 158,489,415-158,893,581 PYHIN5P, OR10X1, 16 more genes
    nsv6333958copy number variation1nstd223human GRCh38 chr1: 158,604,453-158,604,905 , GRCh37.p13 chr1: 158,574,243-158,574,695 OR10Z1
    nsv6316782copy number variation1nstd223human GRCh38 chr1: 158,519,625-158,923,788 , GRCh37.p13 chr1: 158,489,415-158,893,578 HSP90AA3P, OR6K3, 16 more genes
    nsv6290386copy number variation1nstd102humanUncertain significance GRCh37 chr1: 158,489,546-158,889,411 , GRCh38.p12 chr1: 158,519,756-158,919,621 SPTA1, OR6K6, 16 more genes
    nsv6133742copy number variation1nstd213human GRCh37 chr1: 158,430,000-161,510,001 , GRCh38.p12 chr1: 158,460,210-161,540,211 APCS, FCER1A, 174 more genes
    nsv6133741copy number variation1nstd213human GRCh37 chr1: 158,390,000-161,480,001 , GRCh38.p12 chr1: 158,420,210-161,510,211 ATP1A4, CD48, 169 more genes
    nsv6133740copy number variation1nstd213human GRCh37 chr1: 158,330,000-161,530,001 , GRCh38.p12 chr1: 158,360,210-161,560,211 ATP1A2, ATP1A4, 178 more genes
    nsv6133563copy number variation1nstd213human GRCh37 chr1: 156,490,000-159,480,001 , GRCh38.p12 chr1: 156,520,208-159,510,211 CD1A, CD1D, 104 more genes
    nsv6050437insertion1nstd212human GRCh38 chr1: 158,605,736-158,605,736 , GRCh37.p13 chr1: 158,575,526-158,575,526 OR10Z1
    nsv5981880copy number variation1nstd212human GRCh38 chr1: 158,585,335-158,608,315 , GRCh37.p13 chr1: 158,555,125-158,578,105 OR10Z1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4674553copy number variation1nstd102humanUncertain significance GRCh37 chr1: 158,489,545-158,889,411 , GRCh38.p12 chr1: 158,519,755-158,919,621 OR6K2, OR6N2, 16 more genes
    nsv4450412copy number variation1nstd102humanPathogenic GRCh37 chr1: 157,321,299-167,391,423 , GRCh38.p12 chr1: 157,351,509-167,422,186 FCGR3B, SLAMF9, 302 more genes
    nsv4385444copy number variation1nstd173human GRCh37 chr1: 158,214,469-159,706,408 , GRCh38.p12 chr1: 158,244,679-159,736,618 , RAD1P2, 60 more genes
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
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