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Items: 1 to 20 of 93

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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
    nsv7098887copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213 LGI1, LOC107984257, 79 more genes
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7069648inversion1nstd229human GRCh38 chr10: 91,549,162-91,649,153 , GRCh37.p13 chr10: 93,308,919-93,408,910 PPP1R3C, HECTD2-AS1, 1 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv7058955inversion1nstd229human GRCh38 chr10: 91,431,297-91,751,301 , GRCh37.p13 chr10: 93,191,054-93,511,058 PPP1R3C, LOC105378433, 5 more genes
    nsv6889678copy number variation1nstd229human GRCh38 chr10: 91,632,901-91,638,600 , GRCh37.p13 chr10: 93,392,658-93,398,357 PPP1R3C
    nsv6888828copy number variation1nstd229human GRCh38 chr10: 91,599,903-91,735,868 , GRCh37.p13 chr10: 93,359,660-93,495,625 PPP1R3C, HECTD2-AS1, 2 more genes
    nsv6879946copy number variation1nstd229human GRCh38 chr10: 91,626,165-91,633,463 , GRCh37.p13 chr10: 93,385,922-93,393,220 PPP1R3C
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6637542copy number variation1nstd102humanPathogenic GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659 IFIT6P, HECTD2, 166 more genes
    nsv6593400inversion1nstd223human GRCh38 chr10: 91,430,831-91,751,754 , GRCh37.p13 chr10: 93,190,588-93,511,511 PPP1R3C, HECTD2, 5 more genes
    nsv6436604copy number variation1nstd223human GRCh38 chr10: 91,625,118-91,626,799 , GRCh37.p13 chr10: 93,384,875-93,386,556 PPP1R3C
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5630647insertion1nstd207human GRCh38 chr10: 91,633,521-91,633,521 , GRCh37.p13 chr10: 93,393,278-93,393,278 PPP1R3C
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 EIF2S2P3, CYP17A1-AS1, 895 more genes
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