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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7093854copy number variation1nstd102humanUncertain significance GRCh37 chr10: 101,915,882-101,927,183 , GRCh38.p12 chr10: 100,156,125-100,167,426 ERLIN1
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6888931copy number variation1nstd229human GRCh38 chr10: 100,185,904-100,197,365 , GRCh37.p13 chr10: 101,945,661-101,957,122 ERLIN1, CHUK
    nsv6883112copy number variation1nstd229human GRCh38 chr10: 100,152,354-100,154,859 , GRCh37.p13 chr10: 101,912,111-101,914,616 ERLIN1
    nsv6620149copy number variation1nstd224human GRCh37 chr10: 101,880,700-101,916,862 , GRCh38.p12 chr10: 100,120,943-100,157,105 SPCS2P2, CYP2C23P, 1 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6582985inversion1nstd223human GRCh38 chr10: 100,165,925-100,166,301 , GRCh37.p13 chr10: 101,925,682-101,926,058 ERLIN1
    nsv6453414copy number variation1nstd223human GRCh38 chr10: 100,180,801-100,190,000 , GRCh37.p13 chr10: 101,940,558-101,949,757 ERLIN1, CHUK
    nsv6441680copy number variation1nstd223human GRCh38 chr10: 99,317,365-100,480,706 , GRCh37.p13 chr10: 101,077,122-102,240,463 WNT8B, GOT1, 29 more genes
    nsv6440044copy number variation1nstd223human GRCh38 chr10: 100,154,307-100,154,639 , GRCh37.p13 chr10: 101,914,064-101,914,396 ERLIN1
    nsv6247430mobile element insertion1nstd215human GRCh38 chr10: 100,184,278-100,184,278 , GRCh37.p13 chr10: 101,944,035-101,944,035 ERLIN1
    nsv6247429mobile element insertion1nstd215human GRCh38 chr10: 100,178,918-100,178,918 , GRCh37.p13 chr10: 101,938,675-101,938,675 ERLIN1
    nsv6132013copy number variation1nstd213human GRCh37 chr10: 101,250,000-103,200,001 , GRCh38.p12 chr10: 99,490,243-101,440,244 CHUK, ABCC2, 52 more genes
    nsv6131925copy number variation2nstd213human GRCh37 chr10: 101,250,000-103,190,001 , GRCh38.p12 chr10: 99,490,243-101,430,244 CHUK, ABCC2, 52 more genes
    nsv6131845copy number variation1nstd213human GRCh37 chr10: 100,150,000-103,440,001 , GRCh38.p12 chr10: 98,390,243-101,680,244 CHUK, ABCC2, 70 more genes
    nsv6081930insertion1nstd212human GRCh38 chr10: 100,171,090-100,171,090 , GRCh37.p13 chr10: 101,930,847-101,930,847 ERLIN1
    nsv5927417copy number variation1nstd209human GRCh38 chr10: 100,179,709-100,182,281 , GRCh37.p13 chr10: 101,939,466-101,942,038 ERLIN1
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