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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 AGT, MAP10, 221 more genes
    nsv7148158copy number variation1nstd102humanPathogenic GRCh38 chr1: 235,215,476-247,005,888 , GRCh37.p13 chr1: 235,378,791-247,169,190 RNU6-747P, LINC01139, 172 more genes
    nsv7099269copy number variation1nstd231human GRCh38.p12 chr1: 236,539,361-237,579,972 , GRCh37 chr1: 236,702,661-237,743,272 ACTN2, LGALS8, 10 more genes
    nsv7095595copy number variation1nstd102humanUncertain significance GRCh37 chr1: 236,902,582-237,995,947 , GRCh38.p12 chr1: 236,739,282-237,832,647 MIR4428, MT1HL1, 8 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7045904inversion1nstd229human GRCh38 chr1: 236,415,671-241,161,975 , GRCh37.p13 chr1: 236,578,971-241,325,275 PSMD2P1, RN7SKP195, 55 more genes
    nsv7044547inversion1nstd229human GRCh38 chr1: 234,053,817-240,091,334 , GRCh37.p13 chr1: 234,189,563-240,254,634 RNU6-725P, RNU6-968P, 101 more genes
    nsv6666946copy number variation1nstd229human GRCh38 chr1: 236,840,601-237,360,475 , GRCh37.p13 chr1: 237,003,901-237,523,775 RYR2, MT1HL1, 5 more genes
    nsv6661885copy number variation1nstd229human GRCh38 chr1: 236,980,354-237,007,391 , GRCh37.p13 chr1: 237,143,654-237,170,691 RPL35P1, LOC107985368, 1 more genes
    nsv6661037copy number variation1nstd229human GRCh38 chr1: 236,869,826-237,015,359 , GRCh37.p13 chr1: 237,033,126-237,178,659 MTR, RPL35P1, 3 more genes
    nsv6659181copy number variation1nstd229human GRCh38 chr1: 236,988,111-237,029,268 , GRCh37.p13 chr1: 237,151,411-237,192,568 LOC107985368, MT1HL1
    nsv6659136copy number variation1nstd229human GRCh38 chr1: 236,965,611-237,215,759 , GRCh37.p13 chr1: 237,128,911-237,379,059 LOC107985368, RN7SKP195, 3 more genes
    nsv6637109copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,895,447-238,787,061 , GRCh38.p12 chr1: 232,759,701-238,623,761 RPL9P10, LOC105373207, 105 more genes
    nsv6637037copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,827,966-240,750,334 , GRCh38.p12 chr1: 232,692,220-240,587,034 RNU1-74P, EDARADD, 123 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6636217copy number variation1nstd102humanPathogenic GRCh37 chr1: 232,732,121-243,338,216 , GRCh38.p12 chr1: 232,596,375-243,174,914 LINC01347, LOC100130331, 169 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6634337copy number variation1nstd102humanPathogenic GRCh37 chr1: 233,012,994-249,206,918 , GRCh38.p12 chr1: 232,877,248-248,912,719 OR2M4, KIF28P, 316 more genes
    nsv6626216copy number variation1nstd224human GRCh37 chr1: 237,013,670-237,523,573 , GRCh38.p12 chr1: 236,850,370-237,360,273 MTR, RYR2, 5 more genes
    nsv6540441inversion1nstd223human GRCh38 chr1: 237,004,688-237,006,148 , GRCh37.p13 chr1: 237,167,988-237,169,448 MT1HL1
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