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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139857insertion1nstd232human GRCh37.p13 chr10: 99,196,311-99,196,311 , GRCh38.p12 chr10: 97,436,554-97,436,554 EXOSC1
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6895623copy number variation1nstd229human GRCh38 chr10: 97,432,204-97,435,021 , GRCh37.p13 chr10: 99,191,961-99,194,778 EXOSC1, PGAM1
    nsv6889992copy number variation1nstd229human GRCh38 chr10: 97,442,049-97,478,982 , GRCh37.p13 chr10: 99,201,806-99,238,739 EXOSC1, MMS19, 1 more genes
    nsv6880683copy number variation1nstd229human GRCh38 chr10: 97,334,301-97,865,700 , GRCh37.p13 chr10: 99,094,058-99,625,457 FRAT2, LOC105378448, 21 more genes
    nsv6880682copy number variation1nstd229human GRCh38 chr10: 97,224,366-98,323,209 , GRCh37.p13 chr10: 98,984,123-100,082,966 ZDHHC16, RPL34P20, 29 more genes
    nsv6880393copy number variation1nstd229human GRCh38 chr10: 97,245,070-97,586,825 , GRCh37.p13 chr10: 99,004,827-99,346,582 LOC644215, ARHGAP19, 14 more genes
    nsv6637978copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,027,360-99,300,723 , GRCh38.p12 chr10: 97,267,603-97,540,966 RPL12P27, ARHGAP19-SLIT1, 12 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6453721copy number variation1nstd223human GRCh38 chr10: 97,440,163-97,441,681 , GRCh37.p13 chr10: 99,199,920-99,201,438 EXOSC1
    nsv6445203copy number variation1nstd223human GRCh38 chr10: 97,429,271-97,443,959 , GRCh37.p13 chr10: 99,189,028-99,203,716 PGAM1, EXOSC1
    nsv6438388copy number variation1nstd223human GRCh38 chr10: 97,439,007-97,440,227 , GRCh37.p13 chr10: 99,198,764-99,199,984 EXOSC1
    nsv6436260copy number variation1nstd223human GRCh38 chr10: 97,443,675-97,450,041 , GRCh37.p13 chr10: 99,203,432-99,209,798 ZDHHC16, EXOSC1
    nsv6314071copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,070,594-99,445,724 , GRCh38.p12 chr10: 97,310,837-97,685,967 AVPI1, ANKRD2, 15 more genes
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5909034copy number variation1nstd209human GRCh38 chr10: 97,440,959-97,483,202 , GRCh37.p13 chr10: 99,200,716-99,242,959 EXOSC1, MMS19, 1 more genes
    nsv5851103copy number variation1nstd209human GRCh38 chr10: 97,441,026-97,459,470 , GRCh37.p13 chr10: 99,200,783-99,219,227 EXOSC1, MMS19, 1 more genes
    nsv5478096copy number variation1nstd206human GRCh38 chr10: 97,437,504-97,437,612 , GRCh37.p13 chr10: 99,197,261-99,197,369 EXOSC1
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