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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078008inversion1nstd229human GRCh38 chr14: 60,214,891-67,756,686 , GRCh37.p13 chr14: 60,681,609-68,223,403 ATP6V1D, LOC101927756, 129 more genes
    nsv7077538inversion1nstd229human GRCh38 chr14: 63,703,374-67,849,523 , GRCh37.p13 chr14: 64,170,092-68,316,240 RPPH1-2P, SYNE2, 75 more genes
    nsv7077051inversion1nstd229human GRCh38 chr14: 63,334,072-65,942,752 , GRCh37.p13 chr14: 63,800,790-66,409,470 FNTB, PPP1R36, 53 more genes
    nsv7067552inversion1nstd229human GRCh38 chr14: 64,994,108-65,671,112 , GRCh37.p13 chr14: 65,460,826-66,137,830 FNTB, RPL21P7, 15 more genes
    nsv7067078inversion1nstd229human GRCh38 chr14: 65,167,217-66,057,465 , GRCh37.p13 chr14: 65,633,935-66,524,183 LINC02324, RPL21P8, 13 more genes
    nsv7059243inversion1nstd229human GRCh38 chr14: 63,034,368-65,530,331 , GRCh37.p13 chr14: 63,501,086-65,997,049 MIR4706, RNU7-116P, 56 more genes
    nsv7058665inversion1nstd229human GRCh38 chr14: 65,201,079-65,561,098 , GRCh37.p13 chr14: 65,667,797-66,027,816 PTBP1P, RPL21P7, 9 more genes
    nsv6977506copy number variation1nstd229human GRCh38 chr14: 62,671,855-65,773,169 , GRCh37.p13 chr14: 63,138,573-66,239,887 KCNH5, CHURC1-FNTB, 56 more genes
    nsv6963831copy number variation1nstd229human GRCh38 chr14: 65,094,468-65,287,587 , GRCh37.p13 chr14: 65,561,186-65,754,305 PTBP1P, LOC100420096, 6 more genes
    nsv6960974copy number variation1nstd229human GRCh38 chr14: 65,201,001-65,302,700 , GRCh37.p13 chr14: 65,667,719-65,769,418 PTBP1P, LOC100420096, 3 more genes
    nsv6960520copy number variation1nstd229human GRCh38 chr14: 64,700,079-65,240,524 , GRCh37.p13 chr14: 65,166,797-65,707,242 MAX, LINC02324, 15 more genes
    nsv6960350copy number variation1nstd229human GRCh38 chr14: 65,219,954-65,225,506 , GRCh37.p13 chr14: 65,686,672-65,692,224 LINC02324
    nsv6589523inversion1nstd223human GRCh38 chr14: 65,218,067-65,219,476 , GRCh37.p13 chr14: 65,684,785-65,686,194 LINC02324
    nsv6476063copy number variation1nstd223human GRCh38 chr14: 64,354,345-74,200,229 , GRCh37.p13 chr14: 64,821,063-74,666,932 RNU6-240P, COX7A2P1, 196 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6315477copy number variation1nstd102humanUncertain significance GRCh37 chr14: 64,016,496-65,834,490 , GRCh38.p12 chr14: 63,549,778-65,367,772 LOC105370534, RNU7-116P, 43 more genes
    nsv6133134copy number variation1nstd213human GRCh37 chr14: 64,710,000-67,710,001 , GRCh38.p12 chr14: 64,243,282-67,243,284 ESR2, YBX1P1, 46 more genes
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5502709copy number variation1nstd206human GRCh38 chr14: 65,222,055-65,223,124 , GRCh37.p13 chr14: 65,688,773-65,689,842 LINC02324
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
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