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Items: 1 to 20 of 91

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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
    nsv7059243inversion1nstd229human GRCh38 chr14: 63,034,368-65,530,331 , GRCh37.p13 chr14: 63,501,086-65,997,049 MIR4706, RNU7-116P, 56 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
    nsv6974747copy number variation1nstd229human GRCh38 chr14: 64,534,700-64,539,653 , GRCh37.p13 chr14: 65,001,418-65,006,371 HSPA2-AS1, HSPA2
    nsv6971505copy number variation1nstd229human GRCh38 chr14: 64,539,601-64,542,400 , GRCh37.p13 chr14: 65,006,319-65,009,118 HSPA2-AS1, HSPA2
    nsv6622568copy number variation1nstd224human GRCh37 chr14: 65,007,898-65,019,554 , GRCh38.p12 chr14: 64,541,180-64,552,836 HSPA2, PPP1R36
    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
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4729599copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 61,409,856-65,742,610 , GRCh38.p12 chr14: 60,943,138-65,275,892 PARP1P2, ESR2, 73 more genes
    nsv4621034copy number variation1nstd183human GRCh37 chr14: 65,009,995-65,020,189 , GRCh38.p12 chr14: 64,543,277-64,553,471 HSPA2, PPP1R36
    nsv4340065sequence alteration1nstd166human GRCh37.p13 chr14: 63,501,085-66,409,469 , GRCh38.p12 chr14: 63,034,367-65,942,751 , FUT8, 60 more genes
    nsv4217496copy number variation1nstd166human GRCh37.p13 chr14: 65,005,000-65,015,000 , GRCh38.p12 chr14: 64,538,282-64,548,282 HSPA2-AS1, HSPA2, 1 more genes
    nsv3923965copy number variation1nstd102humanPathogenic GRCh37 chr14: 60,383,769-67,217,521 , NCBI36 chr14: 59,453,522-66,287,274 , GRCh38 chr14: 59,917,051-66,750,803 ESR2, PPP2R5E, 111 more genes
    nsv3922652copy number variation1nstd102humanPathogenic GRCh37 chr14: 57,507,754-67,674,948 , NCBI36 chr14: 56,577,507-66,744,701 , GRCh38 chr14: 57,041,036-67,208,231 PARP1P2, SNAPC1, 160 more genes
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