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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070986inversion1nstd229human GRCh38 chr17: 59,331,393-62,738,993 , GRCh37.p13 chr17: 57,408,754-60,816,354 MIR21, LINC01476, 83 more genes
    nsv7062151inversion1nstd229human GRCh38 chr17: 58,705,434-61,610,111 , GRCh37.p13 chr17: 56,782,795-59,687,472 RNU4-13P, LOC105371850, 74 more genes
    nsv6992168copy number variation1nstd229human GRCh38 chr17: 60,088,913-60,187,280 , GRCh37.p13 chr17: 58,166,274-58,264,641 HEATR6-DT, LOC100996660, 5 more genes
    nsv6990398copy number variation1nstd229human GRCh38 chr17: 60,076,885-60,159,093 , GRCh37.p13 chr17: 58,154,246-58,236,454 LOC653653, WFDC21P, 4 more genes
    nsv6988516copy number variation1nstd229human GRCh38 chr17: 60,099,589-60,108,055 , GRCh37.p13 chr17: 58,176,950-58,185,416 LOC653653
    nsv6593672inversion1nstd223human GRCh38 chr17: 60,019,455-60,127,187 , GRCh37.p13 chr17: 58,096,816-58,204,548 HEATR6-DT, WFDC21P, 8 more genes
    nsv6524949copy number variation1nstd223human GRCh38 chr17: 60,101,001-60,106,300 , GRCh37.p13 chr17: 58,178,362-58,183,661 LOC653653
    nsv6523181copy number variation1nstd223human GRCh38 chr17: 60,102,601-60,103,000 , GRCh37.p13 chr17: 58,179,962-58,180,361 LOC653653
    nsv6315566copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 58,111,094-60,323,067 , GRCh38.p12 chr17: 60,033,733-62,245,706 CA4, TBX2, 42 more genes
    nsv6310393copy number variation1nstd102humanUncertain significance GRCh37 chr17: 54,671,585-59,938,900 , GRCh38.p12 chr17: 56,594,224-61,861,539 RNF43, LOC107985048, 132 more genes
    nsv6291649copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,605,300-59,389,547 , GRCh38.p12 chr17: 59,527,939-61,312,186 RNU4-13P, PTRH2, 48 more genes
    nsv6289794copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 58,076,721-60,362,868 , GRCh38.p12 chr17: 59,999,360-62,285,507 CA4, TBX2, 49 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv6110284inversion1nstd212human GRCh37.p13 chr17: 58,096,546-58,188,249 , GRCh38 chr17: 60,019,185-60,110,888 HEATR6, TBC1D3P1, 7 more genes
    nsv5978545inversion1nstd209human GRCh38 chr17: 60,019,388-60,127,177 , GRCh37.p13 chr17: 58,096,749-58,204,538 HEATR6, TBC1D3P1, 8 more genes
    nsv5671151inversion1nstd207human GRCh37.p13 chr17: 58,114,962-58,186,659 , GRCh38 chr17: 60,037,601-60,109,298 HEATR6, WFDC21P, 4 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5530663copy number variation1nstd206human GRCh38 chr17: 60,048,980-60,111,980 , GRCh37.p13 chr17: 58,126,341-58,189,341 WFDC21P, LOC100422693, 3 more genes
    nsv4764279inversion1nstd199human GRCh37 chr17: 58,113,001-58,188,246 , GRCh38.p12 chr17: 60,035,640-60,110,885 HEATR6, WFDC21P, 4 more genes
    nsv4760208inversion1nstd199human GRCh37 chr17: 58,098,217-58,203,052 , GRCh38.p12 chr17: 60,020,856-60,125,691 HEATR6, WFDC21P, 5 more genes
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