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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147072copy number variation1nstd232human GRCh37.p13 chr6: 31,604,911-31,605,007 , GRCh38.p12 chr6: 31,637,134-31,637,230 PRRC2A, BAG6
    nsv7145316copy number variation1nstd232human GRCh37.p13 chr6: 31,604,193-31,604,282 , GRCh38.p12 chr6: 31,636,416-31,636,505 PRRC2A
    nsv7144505insertion1nstd232human GRCh37.p13 chr6: 31,593,940-31,593,940 , GRCh38.p12 chr6: 31,626,163-31,626,163 PRRC2A
    nsv7140484copy number variation1nstd232human GRCh37.p13 chr6: 31,592,135-31,592,223 , GRCh38.p12 chr6: 31,624,358-31,624,446 PRRC2A
    nsv7138474copy number variation1nstd232human GRCh37.p13 chr6: 31,604,720-31,604,815 , GRCh38.p12 chr6: 31,636,943-31,637,038 PRRC2A, BAG6
    nsv7137818copy number variation1nstd232human GRCh37.p13 chr6: 31,603,240-31,603,355 , GRCh38.p12 chr6: 31,635,463-31,635,578 PRRC2A
    nsv7137305insertion1nstd232human GRCh37.p13 chr6: 31,602,755-31,602,755 , GRCh38.p12 chr6: 31,634,978-31,634,978 PRRC2A
    nsv7097426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173 LEMD2, PSORS1C1, 321 more genes
    nsv7097325copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-31,937,492 , GRCh38.p12 chr6: 30,728,116-31,969,715 HCG21, SNORD84, 117 more genes
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv6402266copy number variation1nstd223human GRCh38 chr6: 31,522,086-32,653,908 , GRCh37.p13 chr6: 31,489,863-32,621,685 MIR6833, LY6G5B, 102 more genes
    nsv6400883copy number variation1nstd223human GRCh38 chr6: 31,613,399-31,618,819 , GRCh37.p13 chr6: 31,581,176-31,586,596 PRRC2A, AIF1
    nsv6308333insertion1nstd186human GRCh37 chr6: 31,598,085-31,598,135 , GRCh38.p12 chr6: 31,630,308-31,630,358 PRRC2A
    nsv6304269copy number variation1nstd186human GRCh37 chr6: 31,587,095-31,587,381 , GRCh38.p12 chr6: 31,619,318-31,619,604 PRRC2A
    nsv6289880copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 28,005,012-31,683,185 , GRCh38.p12 chr6: 28,037,234-31,715,408 ABCF1, AIF1, 313 more genes
    nsv6260710mobile element insertion1nstd215human GRCh38 chr6: 31,619,844-31,619,844 , GRCh37.p13 chr6: 31,587,621-31,587,621 PRRC2A
    nsv6135917copy number variation1nstd213human GRCh37 chr6: 30,110,000-32,450,001 , GRCh38.p12 chr6: 30,142,223-32,482,224 ABCF1, AGER, 186 more genes
    nsv6011358copy number variation1nstd212human GRCh38 chr6: 31,619,346-31,619,631 , GRCh37.p13 chr6: 31,587,123-31,587,408 PRRC2A
    nsv5538859insertion1nstd206human GRCh38 chr6: 31,630,308-31,630,358 , GRCh37.p13 chr6: 31,598,085-31,598,135 PRRC2A
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