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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060440inversion1nstd229human GRCh38 chr9: 33,533,890-38,610,880 , GRCh37.p13 chr9: 33,533,888-38,610,877 FRMPD1, PTENP1, 182 more genes
    nsv6869861copy number variation1nstd229human GRCh38 chr9: 38,590,401-38,592,600 , GRCh37.p13 chr9: 38,590,398-38,592,597 ANKRD18A
    nsv6866300copy number variation1nstd229human GRCh38 chr9: 38,451,083-38,640,293 , GRCh37.p13 chr9: 38,451,080-38,640,290 FAM201A, ARMC8P1, 8 more genes
    nsv6866155copy number variation1nstd229human GRCh38 chr9: 38,555,863-38,565,087 , GRCh37.p13 chr9: 38,555,860-38,565,084 ANKRD18A
    nsv6862470copy number variation1nstd229human GRCh38 chr9: 38,555,901-38,567,100 , GRCh37.p13 chr9: 38,555,898-38,567,097 SNX18P3, ANKRD18A
    nsv6862251copy number variation1nstd229human GRCh38 chr9: 38,498,789-38,685,383 , GRCh37.p13 chr9: 38,498,786-38,685,380 YWHABP1, ANKRD18A, 8 more genes
    nsv6858948copy number variation1nstd229human GRCh38 chr9: 37,926,854-38,721,465 , GRCh37.p13 chr9: 37,926,851-38,721,462 CYP4F33P, ANKRD18A, 19 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6633518copy number variation1nstd224human GRCh37 chr9: 38,362,171-38,772,575 , GRCh38.p12 chr9: 38,362,174-38,772,578 FAM201A, ANKRD18A, 15 more genes
    nsv6560363inversion1nstd223human GRCh38 chr9: 33,533,993-38,610,852 , GRCh37.p13 chr9: 33,533,991-38,610,849 PHF24, CNTFR, 182 more genes
    nsv6455414copy number variation1nstd223human GRCh38 chr9: 38,601,762-38,602,349 , GRCh37.p13 chr9: 38,601,759-38,602,346 ANKRD18A
    nsv6444699copy number variation1nstd223human GRCh38 chr9: 38,555,701-38,566,100 , GRCh37.p13 chr9: 38,555,698-38,566,097 SNX18P3, ANKRD18A
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6276618insertion1nstd214human GRCh38 chr9: 38,620,520-38,620,520 , GRCh37.p13 chr9: 38,620,517-38,620,517 FAM201A, ANKRD18A
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
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