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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094921copy number variation1nstd102humanUncertain significance GRCh37 chr17: 76,851,749-78,367,298 , GRCh38.p12 chr17: 78,855,667-80,393,498 RNF213-AS1, EIF4A3, 25 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv6997208copy number variation1nstd229human GRCh38 chr17: 79,046,874-79,050,941 , GRCh37.p13 chr17: 77,042,956-77,047,023 C1QTNF1
    nsv6993964copy number variation1nstd229human GRCh38 chr17: 78,767,102-79,347,128 , GRCh37.p13 chr17: 76,763,184-77,343,210 CYTH1, C1QTNF1-AS1, 9 more genes
    nsv6993667copy number variation1nstd229human GRCh38 chr17: 78,709,580-81,173,842 , GRCh37.p13 chr17: 76,705,662-79,147,642 C1QTNF1-AS1, NPTX1, 47 more genes
    nsv6989484copy number variation1nstd229human GRCh38 chr17: 79,041,988-79,042,519 , GRCh37.p13 chr17: 77,038,070-77,038,601 C1QTNF1
    nsv6988338copy number variation1nstd229human GRCh38 chr17: 79,010,779-79,043,253 , GRCh37.p13 chr17: 77,006,861-77,039,335 C1QTNF1, C1QTNF1-AS1
    nsv6986738copy number variation1nstd229human GRCh38 chr17: 79,030,601-79,053,700 , GRCh37.p13 chr17: 77,026,683-77,049,782 C1QTNF1
    nsv6624116copy number variation1nstd224human GRCh37 chr17: 76,921,790-77,051,253 , GRCh38.p12 chr17: 78,925,708-79,055,171 TIMP2, LGALS3BP, 3 more genes
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6529265copy number variation1nstd223human GRCh38 chr17: 78,919,705-79,477,438 , GRCh37.p13 chr17: 76,915,787-77,412,076 CANT1, C1QTNF1-AS1, 5 more genes
    nsv6528375copy number variation1nstd223human GRCh38 chr17: 79,037,417-79,037,923 , GRCh37.p13 chr17: 77,033,499-77,034,005 C1QTNF1
    nsv6527432copy number variation1nstd223human GRCh38 chr17: 79,031,271-79,031,710 , GRCh37.p13 chr17: 77,027,353-77,027,792 C1QTNF1
    nsv6519219copy number variation1nstd223human GRCh38 chr17: 79,039,369-79,039,686 , GRCh37.p13 chr17: 77,035,451-77,035,768 C1QTNF1
    nsv6517656copy number variation1nstd223human GRCh38 chr17: 79,022,064-79,022,674 , GRCh37.p13 chr17: 77,018,146-77,018,756 C1QTNF1-AS1, C1QTNF1
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6314181copy number variation1nstd102humanUncertain significance GRCh37 chr17: 76,770,309-77,174,429 , GRCh38.p12 chr17: 78,774,227-79,178,347 LGALS3BP, CYTH1, 9 more genes
    nsv6291550copy number variation1nstd102humanUncertain significance GRCh37 chr17: 76,852,379-77,297,300 , GRCh38.p12 chr17: 78,856,297-79,301,218 LGALS3BP, ENGASE, 6 more genes
    nsv6203759copy number variation1nstd214human GRCh38 chr17: 79,030,483-79,030,532 , GRCh37.p13 chr17: 77,026,565-77,026,614 C1QTNF1
    nsv6133425copy number variation1nstd213human GRCh37 chr17: 76,360,000-77,240,001 , GRCh38.p12 chr17: 78,363,919-79,243,919 LGALS3BP, PGS1, 18 more genes
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