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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
    nsv7076231inversion1nstd229human GRCh38 chr17: 69,015,631-73,552,061 , GRCh37.p13 chr17: 67,011,772-71,548,200 KCNJ2-AS1, ROCR, 52 more genes
    nsv7066890inversion1nstd229human GRCh38 chr17: 70,169,508-70,169,607 , GRCh37.p13 chr17: 68,165,649-68,165,748 KCNJ2, KCNJ2-AS1
    nsv7059395inversion1nstd229human GRCh38 chr17: 70,155,641-70,192,608 , GRCh37.p13 chr17: 68,151,782-68,188,749 LOC105371882, KCNJ2-AS1, 1 more genes
    nsv6638043copy number variation1nstd102humanUncertain significance GRCh37 chr17: 67,730,594-68,272,354 , GRCh38.p12 chr17: 69,734,453-70,276,213 LINC01483, KCNJ2, 8 more genes
    nsv6524723copy number variation1nstd223human GRCh38 chr17: 70,168,601-70,169,700 , GRCh37.p13 chr17: 68,164,742-68,165,841 KCNJ2-AS1, KCNJ2
    nsv6310233copy number variation2nstd102humanUncertain significance GRCh37 chr17: 68,171,181-68,172,464 , GRCh38.p12 chr17: 70,175,040-70,176,323 KCNJ2
    nsv6290572copy number variation1nstd102humanUncertain significance GRCh38 chr17: 70,166,313-70,176,696 , GRCh37.p13 chr17: 68,162,454-68,172,837 KCNJ2-AS1, KCNJ2
    nsv6133070copy number variation1nstd213human GRCh37 chr17: 62,460,000-73,800,001 , GRCh38.p12 chr17: 64,464,645-75,803,920 APOH, CACNG1, 225 more genes
    nsv5707600mobile element insertion1nstd211human GRCh38 chr17: 70,177,511-70,177,511 , GRCh37.p13 chr17: 68,173,652-68,173,652 KCNJ2
    nsv5419026mobile element insertion1nstd206human GRCh38 chr17: 70,177,511-70,177,562 , GRCh37.p13 chr17: 68,173,652-68,173,703 KCNJ2
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv4769306copy number variation1nstd102humanPathogenic GRCh37 chr17: 68,166,871-68,171,602 , GRCh38 chr17: 70,170,730-70,175,461 KCNJ2
    nsv4676102copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 68,056,381-68,268,736 , GRCh38.p12 chr17: 70,060,240-70,272,595 KCNJ2, KCNJ16, 5 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4378806copy number variation1nstd173human GRCh37 chr17: 67,438,891-68,743,388 , GRCh38.p12 chr17: 69,442,750-70,747,247 , LINC01028, 11 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv3972399copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 64,159,738-74,891,024 , GRCh38.p12 chr17: 66,163,620-76,894,942 AANAT, ACOX1, 243 more genes
    nsv3923674copy number variation1nstd102humanLikely benign NCBI36 chr17: 65,596,853-66,619,160 , GRCh37 chr17: 68,085,258-69,107,565 , GRCh38 chr17: 70,089,117-71,111,424 KCNJ2, LOC100131241, 6 more genes
    nsv3921648copy number variation1nstd102humanUncertain significance GRCh37 chr17: 68,090,109-68,705,937 , GRCh38 chr17: 70,093,968-70,709,796 , NCBI36 chr17: 65,601,704-66,217,532 KCNJ16, KCNJ2-AS1, 3 more genes
    nsv3919156copy number variation1nstd102humanPathogenic GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717 CD300A, RNF213, 359 more genes
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