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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054901inversion1nstd229human GRCh38 chr5: 86,506,255-87,299,369 , GRCh37.p13 chr5: 85,802,072-86,595,186 RN7SL629P, MIR4280, 12 more genes
    nsv7053596inversion1nstd229human GRCh38 chr5: 85,730,857-88,063,519 , GRCh37.p13 chr5: 85,026,675-87,359,336 LOC100421863, RPL10AP9, 25 more genes
    nsv7050687inversion1nstd229human GRCh38 chr5: 86,603,498-87,299,362 , GRCh37.p13 chr5: 85,899,315-86,595,179 RPL10AP9, LINC01949, 12 more genes
    nsv7041118inversion1nstd229human GRCh38 chr5: 87,205,997-87,214,600 , GRCh37.p13 chr5: 86,501,814-86,510,417 LINC01949, LOC101929380
    nsv7038903inversion1nstd229human GRCh38 chr5: 87,228,608-87,228,659 , GRCh37.p13 chr5: 86,524,425-86,524,476 LINC01949, LOC101929380
    nsv6770648copy number variation1nstd229human GRCh38 chr5: 87,125,326-87,231,724 , GRCh37.p13 chr5: 86,421,143-86,527,541 LOC101929380, LINC01949
    nsv6769207copy number variation1nstd229human GRCh38 chr5: 87,225,700-87,226,703 , GRCh37.p13 chr5: 86,521,517-86,522,520 LOC101929380, LINC01949
    nsv6763944copy number variation1nstd229human GRCh38 chr5: 87,221,401-87,224,200 , GRCh37.p13 chr5: 86,517,218-86,520,017 LINC01949, LOC101929380
    nsv6762944copy number variation1nstd229human GRCh38 chr5: 87,046,508-87,930,460 , GRCh37.p13 chr5: 86,342,325-87,226,277 LINC02488, LOC105379065, 13 more genes
    nsv6760025copy number variation1nstd229human GRCh38 chr5: 86,980,801-87,434,400 , GRCh37.p13 chr5: 86,276,618-86,730,217 LOC105379065, RN7SL629P, 11 more genes
    nsv6630450copy number variation1nstd224human GRCh37 chr5: 86,478,799-86,511,450 , GRCh38.p12 chr5: 87,182,982-87,215,633 LOC101929380, LINC01949
    nsv6568909inversion1nstd223human GRCh38 chr5: 87,221,092-87,221,546 , GRCh37.p13 chr5: 86,516,909-86,517,363 LINC01949, LOC101929380
    nsv6407740copy number variation1nstd223human GRCh38 chr5: 87,234,850-87,235,408 , GRCh37.p13 chr5: 86,530,667-86,531,225 LINC01949, LOC101929380
    nsv6404497copy number variation1nstd223human GRCh38 chr5: 87,181,314-87,220,845 , GRCh37.p13 chr5: 86,477,131-86,516,662 LINC01949, LOC101929380
    nsv6313788copy number variation1nstd102humanPathogenic GRCh37 chr5: 82,185,951-90,110,454 , GRCh38.p12 chr5: 82,890,132-90,814,637 RASA1, HAPLN1, 82 more genes
    nsv6313570copy number variation1nstd102humanPathogenic GRCh37 chr5: 86,426,877-86,614,352 , GRCh38.p12 chr5: 87,131,060-87,318,535 CCNH, RASA1, 5 more genes
    nsv6244497mobile element insertion1nstd215human GRCh38 chr5: 87,239,080-87,239,080 , GRCh37.p13 chr5: 86,534,897-86,534,897 LINC01949, LOC101929380
    nsv6171649copy number variation1nstd214human GRCh38 chr5: 87,231,135-87,231,224 , GRCh37.p13 chr5: 86,526,952-86,527,041 LOC101929380, LINC01949
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135200copy number variation1nstd213human GRCh37 chr5: 76,540,000-94,260,001 , GRCh38.p12 chr5: 77,244,175-94,924,296 ACTBP2, ARSB, 200 more genes
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