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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6644889copy number variation1nstd229human GRCh38 chr1: 173,847,349-173,921,917 , GRCh37.p13 chr1: 173,816,487-173,891,055 DARS2, SNORD76, 15 more genes
    nsv6644717copy number variation1nstd229human GRCh38 chr1: 172,496,006-174,441,202 , GRCh37.p13 chr1: 172,465,146-174,410,340 RABGAP1L-DT, LOC100506023, 46 more genes
    nsv6644381copy number variation1nstd229human GRCh38 chr1: 173,863,983-173,867,554 , GRCh37.p13 chr1: 173,833,121-173,836,692 SNORD76, SNORD74, 12 more genes
    nsv6625682copy number variation1nstd224human GRCh37 chr1: 173,796,169-173,995,161 , GRCh38.p12 chr1: 173,827,031-174,026,023 SNORD79, SNORD47, 18 more genes
    nsv6313831copy number variation1nstd102humanUncertain significance GRCh37 chr1: 173,750,496-174,538,509 , GRCh38.p12 chr1: 173,781,358-174,569,371 SNORD47, SNORD76, 27 more genes
    nsv6313519copy number variation1nstd102humanPathogenic GRCh37 chr1: 171,881,608-175,899,893 , GRCh38.p12 chr1: 171,912,468-175,930,757 RNU6-693P, PIGC, 73 more genes
    nsv6310765copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr1: 171,605,065-173,962,123 , GRCh38.p12 chr1: 171,635,925-173,992,985 RNU6-157P, SNORD47, 60 more genes
    nsv6289986copy number variation1nstd102humanPathogenic GRCh38 chr1: 173,501,975-175,305,010 , GRCh37.p13 chr1: 173,471,114-175,274,146 GAS5-AS1, ENTR1P2, 44 more genes
    nsv6289891copy number variation1nstd102humanPathogenic GRCh38 chr1: 172,987,296-174,843,232 , GRCh37.p13 chr1: 172,956,436-174,812,370 LOC100302291, SNORD75, 41 more genes
    nsv6289884copy number variation1nstd102humanPathogenic GRCh38 chr1: 173,848,142-174,816,147 , GRCh37.p13 chr1: 173,817,280-174,785,285 SNORD75, SNORD78, 25 more genes
    nsv6289881copy number variation1nstd102humanPathogenic GRCh38 chr1: 173,859,535-173,926,473 , GRCh37.p13 chr1: 173,828,673-173,895,611 SNORD77, SNORD44, 14 more genes
    nsv6289872copy number variation1nstd102humanPathogenic GRCh38 chr1: 173,686,375-176,083,118 , GRCh37.p13 chr1: 173,655,514-176,052,254 ENTR1P2, GAS5-AS1, 49 more genes
    nsv6289861copy number variation1nstd102humanPathogenic GRCh38 chr1: 173,787,361-174,223,422 , GRCh37.p13 chr1: 173,756,499-174,192,560 SNORD76, SNORD75, 24 more genes
    nsv6289797copy number variation1nstd102humanPathogenic GRCh38 chr1: 173,850,996-173,950,174 , GRCh37.p13 chr1: 173,820,134-173,919,312 SNORD76, SNORD47, 16 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133749copy number variation1nstd213human GRCh37 chr1: 173,530,000-175,550,001 , GRCh38.p12 chr1: 173,560,861-175,580,865 SERPINC1, KIAA0040, 46 more genes
    nsv6133573copy number variation1nstd213human GRCh37 chr1: 173,820,000-189,960,001 , GRCh38.p12 chr1: 173,850,862-189,990,871 ABL2, ASTN1, 235 more genes
    nsv6133567copy number variation1nstd213human GRCh37 chr1: 170,760,000-174,730,001 , GRCh38.p12 chr1: 170,790,859-174,760,863 FASLG, SERPINC1, 87 more genes
    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
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