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Items: 1 to 20 of 208

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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
    nsv6873425copy number variation1nstd229human GRCh38 chr9: 97,324,318-97,349,786 , GRCh37.p13 chr9: 100,086,600-100,112,068 SUGT1P4-STRA6LP-CCDC180, CCDC180
    nsv6872305copy number variation1nstd229human GRCh38 chr9: 97,311,184-97,345,574 , GRCh37.p13 chr9: 100,073,466-100,107,856 CCDC180, SUGT1P4-STRA6LP-CCDC180
    nsv6871649copy number variation1nstd229human GRCh38 chr9: 97,318,864-97,340,963 , GRCh37.p13 chr9: 100,081,146-100,103,245 SUGT1P4-STRA6LP-CCDC180, CCDC180
    nsv6869968copy number variation1nstd229human GRCh38 chr9: 97,334,501-97,357,700 , GRCh37.p13 chr9: 100,096,783-100,119,982 SUGT1P4-STRA6LP-CCDC180, CCDC180
    nsv6869737copy number variation1nstd229human GRCh38 chr9: 97,308,401-97,311,646 , GRCh37.p13 chr9: 100,070,683-100,073,928 SUGT1P4-STRA6LP-CCDC180, CCDC180
    nsv6869563copy number variation1nstd229human GRCh38 chr9: 97,344,549-97,352,880 , GRCh37.p13 chr9: 100,106,831-100,115,162 SUGT1P4-STRA6LP-CCDC180, CCDC180
    nsv6867111copy number variation1nstd229human GRCh38 chr9: 97,378,543-97,383,363 , GRCh37.p13 chr9: 100,140,825-100,145,645 CCDC180
    nsv6862162copy number variation1nstd229human GRCh38 chr9: 97,358,651-97,375,642 , GRCh37.p13 chr9: 100,120,933-100,137,924 CCDC180, SUGT1P4-STRA6LP-CCDC180, 1 more genes
    nsv6861096copy number variation1nstd229human GRCh38 chr9: 97,302,701-97,408,400 , GRCh37.p13 chr9: 100,064,983-100,170,682 LOC286359, CCDC180, 2 more genes
    nsv6861071copy number variation1nstd229human GRCh38 chr9: 97,311,865-97,314,743 , GRCh37.p13 chr9: 100,074,147-100,077,025 CCDC180, SUGT1P4-STRA6LP-CCDC180
    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
    nsv6446794copy number variation1nstd223human GRCh38 chr9: 97,344,548-97,352,879 , GRCh37.p13 chr9: 100,106,830-100,115,161 CCDC180, SUGT1P4-STRA6LP-CCDC180
    nsv6445644copy number variation1nstd223human GRCh38 chr9: 97,322,991-97,323,358 , GRCh37.p13 chr9: 100,085,273-100,085,640 SUGT1P4-STRA6LP-CCDC180, CCDC180
    nsv6440502copy number variation1nstd223human GRCh38 chr9: 97,357,001-97,360,687 , GRCh37.p13 chr9: 100,119,283-100,122,969 CCDC180, SUGT1P4-STRA6LP-CCDC180
    nsv6439997copy number variation1nstd223human GRCh38 chr9: 97,318,863-97,340,961 , GRCh37.p13 chr9: 100,081,145-100,103,243 CCDC180, SUGT1P4-STRA6LP-CCDC180
    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
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