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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5192729mobile element insertion1nstd203human GRCh38 chr1: 93,899,076-93,899,076 , GRCh37.p13 chr1: 94,364,632-94,364,632 GCLM
    nsv5077282mobile element insertion1nstd203human GRCh38 chr1: 93,883,274-93,883,274 , GRCh37.p13 chr1: 94,348,830-94,348,830 GCLM
    nsv5074517mobile element insertion1nstd203human GRCh38 chr1: 93,883,273-93,883,273 , GRCh37.p13 chr1: 94,348,829-94,348,829 GCLM
    nsv5063034mobile element insertion1nstd203human GRCh38 chr1: 93,898,303-93,898,303 , GRCh37.p13 chr1: 94,363,859-94,363,859 GCLM
    nsv4897023copy number variation1nstd200human GRCh38 chr1: 93,885,000-93,891,114 , GRCh37.p13 chr1: 94,350,556-94,356,670 GCLM
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    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
    nsv4728160copy number variation1nstd102humanUncertain significance GRCh37 chr1: 94,216,477-94,471,075 , GRCh38.p12 chr1: 93,750,921-94,005,519 MTCO1P21, BCAR3, 11 more genes
    nsv4683510copy number variation1nstd102humanUncertain significance GRCh37 chr1: 94,374,594-94,528,873 , GRCh38.p12 chr1: 93,909,038-94,063,317 MTATP6P13, CHCHD2P5, 7 more genes
    nsv4674663copy number variation1nstd102humanUncertain significance GRCh37 chr1: 93,863,518-96,108,930 , GRCh38.p12 chr1: 93,397,961-95,643,374 CNN3, SLC44A3-AS1, 48 more genes
    nsv4571611mobile element insertion1nstd166human GRCh37.p13 chr1: 94,364,620-94,364,620 , GRCh38.p12 chr1: 93,899,064-93,899,064 GCLM
    nsv4558787inversion1nstd166human GRCh37.p13 chr1: 94,370,379-95,022,629 , GRCh38.p12 chr1: 93,904,823-94,557,073 , RN7SL440P, 17 more genes
    nsv4534728insertion1nstd166human GRCh37.p13 chr1: 94,372,577-94,372,577 , GRCh38.p12 chr1: 93,907,021-93,907,021 GCLM
    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
    nsv4376642copy number variation1nstd173human GRCh37 chr1: 94,318,231-94,440,182 , GRCh38.p12 chr1: 93,852,675-93,974,626 MTCO3P21, MTCO2P21, 7 more genes
    nsv4330538inversion1nstd166human GRCh37.p13 chr1: 94,223,082-113,632,613 , GRCh38.p12 chr1: 93,757,526-113,089,991 , AMPD2, 329 more genes
    nsv3964520copy number variation1nstd168human GRCh38 chr1: 93,795,142-93,915,079 , GRCh37.p13 chr1: 94,260,698-94,380,635 BCAR3, GCLM, 3 more genes
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