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Items: 1 to 20 of 146

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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
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6450925copy number variation1nstd223human GRCh38 chr9: 99,905,401-99,907,300 , GRCh37.p13 chr9: 102,667,683-102,669,582 STX17-DT, STX17
    nsv6449703copy number variation1nstd223human GRCh38 chr9: 99,906,553-99,908,251 , GRCh37.p13 chr9: 102,668,835-102,670,533 STX17, STX17-DT
    nsv6448446copy number variation1nstd223human GRCh38 chr9: 99,903,601-99,909,100 , GRCh37.p13 chr9: 102,665,883-102,671,382 STX17-DT, STX17
    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
    nsv6439936copy number variation1nstd223human GRCh38 chr9: 99,906,401-99,906,900 , GRCh37.p13 chr9: 102,668,683-102,669,182 STX17-DT, STX17
    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
    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
    nsv6141425copy number variation1nstd206human GRCh38 chr9: 99,900,982-99,903,035 , GRCh37.p13 chr9: 102,663,264-102,665,317 STX17-DT
    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
    nsv6097836insertion1nstd212human GRCh38 chr9: 99,886,900-99,886,900 , GRCh37.p13 chr9: 102,649,182-102,649,182 STX17-DT
    nsv6097066insertion1nstd212human GRCh38 chr9: 99,903,612-99,903,612 , GRCh37.p13 chr9: 102,665,894-102,665,894 STX17-DT
    nsv6003709copy number variation1nstd212human GRCh38 chr9: 99,901,118-99,902,696 , GRCh37.p13 chr9: 102,663,400-102,664,978 STX17-DT
    nsv5909366copy number variation1nstd209human GRCh38 chr9: 99,903,540-99,903,617 , GRCh37.p13 chr9: 102,665,822-102,665,899 STX17-DT
    nsv5706562mobile element insertion1nstd211human GRCh38 chr9: 99,886,910-99,886,910 , GRCh37.p13 chr9: 102,649,192-102,649,192 STX17-DT
    nsv5542944insertion1nstd206human GRCh38 chr9: 99,903,490-99,903,540 , GRCh37.p13 chr9: 102,665,772-102,665,822 STX17-DT
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