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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077537inversion1nstd229human GRCh38 chr17: 64,968,697-68,255,761 , GRCh37.p13 chr17: 62,964,815-65,936,105 SNORA38B, PRKCA-AS1, 52 more genes
    nsv7070779inversion1nstd229human GRCh38 chr17: 64,711,213-68,088,947 , GRCh37.p13 chr17: 62,707,331-65,936,105 MICOS10P2, LOC100420638, 61 more genes
    nsv7070446inversion1nstd229human GRCh38 chr17: 65,003,854-68,220,374 , GRCh37.p13 chr17: 62,999,972-65,936,105 SH3GL1P3, AXIN2, 51 more genes
    nsv7059173inversion1nstd229human GRCh38 chr17: 65,003,895-68,220,334 , GRCh37.p13 chr17: 63,000,013-65,936,105 RPSAP67, HELZ-AS1, 51 more genes
    nsv6978104copy number variation1nstd229human GRCh38 chr17: 67,047,649-67,049,902 , GRCh37.p13 chr17: 65,043,765-65,046,018 CACNG1
    nsv6250958mobile element insertion1nstd215human GRCh38 chr17: 67,050,882-67,050,882 , GRCh37.p13 chr17: 65,046,998-65,046,998 CACNG1
    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
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5537123insertion1nstd206human GRCh38 chr17: 67,056,981-67,057,031 , GRCh37.p13 chr17: 65,053,097-65,053,147 CACNG1
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv4676190copy number variation1nstd102humanUncertain significance GRCh37 chr17: 65,050,304-65,440,440 , GRCh38.p12 chr17: 67,054,188-67,444,324 PITPNC1, HELZ, 5 more genes
    nsv4457799copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,869,604-67,078,443 , GRCh38.p12 chr17: 59,792,243-69,082,302 PECAM1, TBX2-AS1, 215 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
    nsv4349383copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,357,088-66,306,668 , GRCh38.p12 chr17: 59,279,727-68,310,527 FAM136DP, HELZ, 214 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
    nsv4264171copy number variation1nstd166human GRCh37.p13 chr17: 65,051,030-65,051,116 , GRCh38.p12 chr17: 67,054,914-67,055,000 CACNG1
    nsv4254209copy number variation1nstd166human GRCh37.p13 chr17: 65,044,227-65,054,375 , GRCh38.p12 chr17: 67,048,111-67,058,259 CACNG1
    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
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3914737copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,649,313-65,683,004 , NCBI36 chr17: 60,061,351-63,113,466 , GRCh38 chr17: 64,634,771-67,686,888 AXIN2, RNU7-115P, 53 more genes
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