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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099018copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-2,580,976 , GRCh38.p12 chr1: 10,001-2,649,537 DVL1, LOC100129534, 148 more genes
    nsv6138155copy number variation1nstd206human GRCh38 chr1: 452,000-458,000 , GRCh37.p13 chr1: 361,337-367,337 OR4F29, LOC112268260
    nsv4728187copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-5,592,835 , GRCh38.p12 chr1: 10,001-5,532,775 UBE2J2, MRPL20, 196 more genes
    nsv4674646copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-3,349,513 , GRCh38.p12 chr1: 82,154-3,432,949 PRKCZ-AS1, PRKCZ, 156 more genes
    nsv4661876copy number variation2nstd186human GRCh37 chr1: 40,718-731,985 , GRCh38.p12 chr1: 40,718-796,605 , OR4F29, 36 more genes
    nsv4649420copy number variation1nstd186human GRCh37 chr1: 364,000-401,750 , GRCh38.p12 chr1: 417,587-455,337 OR4F29, WBP1LP7, 1 more genes
    nsv4594490copy number variation1nstd183human GRCh37 chr1: 351,377-404,070 , GRCh38.p12 chr1: 415,267-467,960 WBP1LP7, LOC112268260, 1 more genes
    nsv4581209copy number variation2nstd183human GRCh37 chr1: 40,718-731,985 , GRCh38.p12 chr1: 40,718-796,605 , OR4G11P, 36 more genes
    nsv4581187copy number variation2nstd183human GRCh37 chr1: 359,638-470,259 , GRCh38.p12 chr1: 349,078-459,699 LOC112268260, OR4F29, 1 more genes
    nsv4581173copy number variation1nstd183human GRCh37 chr1: 317,770-471,337 , GRCh38.p12 chr1: 348,000-501,567 RPL23AP24, OR4F29, 5 more genes
    nsv4436105copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061 PARK7, RNF223, 325 more genes
    nsv4435992copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-7,637,060 , GRCh38.p12 chr1: 82,154-7,577,000 SNORD167, SEPTIN14P14, 222 more genes
    nsv4410074copy number variation1nstd174human GRCh37 chr1: 317,770-471,337 , GRCh38.p12 chr1: 348,000-501,567 RPL23AP24, OR4F29, 5 more genes
    nsv4407951copy number variation1nstd174human GRCh37 chr1: 348,092-461,014 , GRCh38.p12 chr1: 358,323-471,245 LOC112268260, OR4F29, 1 more genes
    nsv4402293copy number variation1nstd174human GRCh37 chr1: 350,531-435,382 , GRCh38.p12 chr1: 383,955-468,806 OR4F29, WBP1LP7, 1 more genes
    nsv4050917copy number variation1nstd166human GRCh37.p13 chr1: 364,000-401,750 , GRCh38.p12 chr1: 417,587-455,337 LOC112268260, WBP1LP7, 1 more genes
    nsv3970365insertion1nstd168human GRCh38 chr1: 348,240-449,940 , GRCh37.p13 chr1: 369,397-471,097 RPL23AP24, OR4F29, 2 more genes
    nsv3924689copy number variation1nstd102humanPathogenic NCBI36 chr1: 4,737-7,449,889 , GRCh37.p13 chr1: 14,874-7,527,302 , GRCh38.p12 chr1: 14,874-7,467,242 MIR6726, PLCH2, 230 more genes
    nsv3917903copy number variation1nstd102humanBenign NCBI36 chr1: 218,560-639,581 , GRCh37.p13 chr1: 228,697-649,718 , GRCh38.p12 chr1: 258,946-714,338 LOC105378947, LOC112268260, 19 more genes
    nsv3913374copy number variation1nstd102humanPathogenic NCBI36 chr1: 4,737-8,767,973 , GRCh37.p13 chr1: 14,874-8,845,386 , GRCh38.p12 chr1: 14,874-8,785,327 LOC105378593, TNFRSF9, 252 more genes
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