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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099219copy number variation1nstd231human GRCh38.p12 chr1: 99,594,616-101,416,026 , GRCh37 chr1: 100,060,172-101,881,582 AGL, DBT, 38 more genes
    nsv7095681copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,316,599-101,709,564 , GRCh38.p12 chr1: 99,851,043-101,244,008 SLC35A3, S1PR1-DT, 29 more genes
    nsv7095304copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,928,187-101,005,677 , GRCh38.p12 chr1: 100,462,631-100,540,121 GPR88, CDC14A
    nsv7044488inversion1nstd229human GRCh38 chr1: 100,052,919-109,025,639 , GRCh37.p13 chr1: 100,518,475-109,568,261 LOC102723784, DNAJA1P5, 109 more genes
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
    nsv6290366copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,215,607-105,368,230 , GRCh38.p12 chr1: 99,750,051-104,825,608 LOC105379827, RPSAP19, 63 more genes
    nsv6133669copy number variation1nstd213human GRCh37 chr1: 95,900,000-101,030,001 , GRCh38.p12 chr1: 95,434,444-100,564,445 PALMD, LRRC39, 56 more genes
    nsv4906389copy number variation1nstd200human GRCh38 chr1: 100,542,317-100,543,480 , GRCh37.p13 chr1: 101,007,873-101,009,036 GPR88
    nsv4788845copy number variation1nstd200human GRCh37 chr1: 101,007,873-101,009,036 , GRCh38.p12 chr1: 100,542,317-100,543,480 GPR88
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4745469copy number variation1nstd199human GRCh37 chr1: 86,005,697-146,486,085 , GRCh38.p12 chr1: 85,540,014-149,528,945 , TAF13, 920 more genes
    nsv4679627copy number variation1nstd189human GRCh37.p13 chr1: 100,661,887-101,495,928 , GRCh38.p12 chr1: 100,196,331-101,030,372 DBT, EXTL2, 18 more genes
    nsv4674470copy number variation1nstd102humanUncertain significance GRCh37 chr1: 100,704,867-101,205,009 , GRCh38.p12 chr1: 100,239,311-100,739,453 RTCA-AS1, RTCA, 11 more genes
    nsv4578855copy number variation1nstd183human GRCh37 chr1: 100,929,502-101,196,287 , GRCh38.p12 chr1: 100,463,946-100,730,731 VCAM1, CDC14A, 4 more genes
    nsv4578705copy number variation2nstd183human GRCh37 chr1: 101,004,688-101,005,733 , GRCh38.p12 chr1: 100,539,132-100,540,177 GPR88
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4406833copy number variation1nstd174human GRCh37 chr1: 101,004,249-101,005,733 , GRCh38.p12 chr1: 100,538,693-100,540,177 GPR88
    nsv4330538inversion1nstd166human GRCh37.p13 chr1: 94,223,082-113,632,613 , GRCh38.p12 chr1: 93,757,526-113,089,991 , AMPD2, 329 more genes
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