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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv6637435copy number variation1nstd102humanUncertain significance GRCh37 chr9: 101,179,298-101,680,286 , GRCh38.p12 chr9: 98,417,016-98,918,004 GALNT12, GABBR2, 4 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
    nsv6447755copy number variation1nstd223human GRCh38 chr9: 92,901,749-100,255,234 , GRCh37.p13 chr9: 95,664,031-103,017,516 EIF4BP3, VN1R51P, 162 more genes
    nsv6440081copy number variation1nstd223human GRCh38 chr9: 98,761,901-98,763,900 , GRCh37.p13 chr9: 101,524,183-101,526,182 ANKS6
    nsv6439111copy number variation1nstd223human GRCh38 chr9: 98,789,501-98,815,900 , GRCh37.p13 chr9: 101,551,783-101,578,182 ANKS6, GALNT12
    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
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 SUGT1P4-STRA6LP, NR4A3, 255 more genes
    nsv6314738copy number variation2nstd102humanUncertain significance, Likely benign GRCh37 chr9: 101,470,679-101,611,374 , GRCh38.p12 chr9: 98,708,397-98,849,092 ANKS6, GALNT12, 1 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 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
    nsv6312742copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 100,190,748-103,062,956 , GRCh38.p12 chr9: 97,428,466-100,300,674 FOXE1, LOC107987011, 47 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
    nsv6136089copy number variation1nstd213human GRCh37 chr9: 100,650,000-102,930,001 , GRCh38.p12 chr9: 97,887,718-100,167,719 TGFBR1, NR4A3, 36 more genes
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5372870translocation1nstd200human GRCh38 chr9: 98,794,157-98,794,157 , GRCh38 chr9: 98,794,735-98,794,735 , GRCh37.p13 chr9: 101,556,439-101,556,439 , GRCh37.p13 chr9: 101,557,017-101,557,017 ANKS6
    nsv5368936translocation1nstd200human GRCh38 chr5: 131,058,349-131,058,349 , GRCh38 chr9: 98,788,768-98,788,768 , GRCh37.p13 chr5: 130,394,042-130,394,042 , GRCh37.p13 chr9: 101,551,050-101,551,050 LOC105379172, ANKS6
    nsv5130407mobile element insertion1nstd203human GRCh38 chr9: 98,778,712-98,778,712 , GRCh37.p13 chr9: 101,540,994-101,540,994 ANKS6
    nsv4982730copy number variation1nstd200human GRCh38 chr9: 98,788,214-98,788,264 , GRCh37.p13 chr9: 101,550,496-101,550,546 ANKS6
    nsv4824202copy number variation1nstd200human GRCh37 chr9: 101,501,666-101,501,824 , GRCh38.p12 chr9: 98,739,384-98,739,542 ANKS6
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