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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137123copy number variation1nstd102humanPathogenic GRCh37 chr8: 89,179,899-97,978,274 , GRCh38.p12 chr8: 88,167,670-96,966,046 SLC26A7, LOC105375639, 112 more genes
    nsv7078060inversion1nstd229human GRCh38 chr8: 88,934,395-91,030,131 , GRCh37.p13 chr8: 89,946,624-92,042,359 RNA5SP273, LOC105375631, 21 more genes
    nsv7063775inversion1nstd229human GRCh38 chr8: 90,028,515-91,181,513 , GRCh37.p13 chr8: 91,040,743-92,193,741 LOC107986955, OTUD6B-AS1, 15 more genes
    nsv6857698copy number variation1nstd229human GRCh38 chr8: 89,506,124-90,615,140 , GRCh37.p13 chr8: 90,518,353-91,627,368 LOC107986955, RNU6-925P, 12 more genes
    nsv6851829copy number variation1nstd229human GRCh38 chr8: 90,072,204-90,078,063 , GRCh37.p13 chr8: 91,084,432-91,090,291 CALB1
    nsv6845087copy number variation1nstd229human GRCh38 chr8: 90,060,175-90,060,380 , GRCh37.p13 chr8: 91,072,403-91,072,608 CALB1
    nsv6637803copy number variation1nstd102humanUncertain significance GRCh37 chr8: 87,010,235-91,879,538 , GRCh38.p12 chr8: 85,998,006-90,867,310 LOC105375633, NTAN1P2, 49 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6555776inversion1nstd223human GRCh38 chr8: 90,046,984-91,196,055 , GRCh37.p13 chr8: 91,059,212-92,208,283 CPP, TMEM64, 15 more genes
    nsv6429148copy number variation1nstd223human GRCh38 chr8: 90,056,956-90,057,267 , GRCh37.p13 chr8: 91,069,184-91,069,495 CALB1
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314425complex chromosomal rearrangement13nstd102humanUncertain significance GRCh37 chr7: 117,503,036-117,503,036 , GRCh37 chr8: 91,069,395-91,069,395 , GRCh37 chr8: 95,362,546-95,362,546 , GRCh37 chr16: 76,871,567-76,871,567 , GRCh37 chr2: 151,153,642-151,153,642 , GRCh37 chr7: 116,774,853-116,774,853 , GRCh37 chr7: 117,591,182-117,591,182 , GRCh37 chr7: 117,591,191-117,591,191 , GRCh37 chr7: 117,641,509-117,641,509 , GRCh37 chr7: 117,641,512-117,641,512 , GRCh37 chr8: 90,305,781-90,305,781 , GRCh37 chr8: 90,305,784-90,305,784 , GRCh37 chr8: 91,070,654-91,070,654 , GRCh37 chr8: 95,362,538-95,362,538 , GRCh37 chr16: 76,871,038-76,871,038 , GRCh37 chr3: 178,446,407-178,446,407 , GRCh37 chr7: 116,774,867-116,774,867 , GRCh37 chr8: 91,069,404-91,069,404 , GRCh37 chr8: 91,070,391-91,070,391 , GRCh37 chr16: 74,546,853-74,546,853 , GRCh37 chr16: 74,546,862-74,546,862 , GRCh37 chr2: 151,153,618-151,153,618 , GRCh37 chr3: 178,446,420-178,446,420 , GRCh37 chr7: 117,539,386-117,539,386 , GRCh37 chr8: 91,661,237-91,661,237 , GRCh37 chr8: 91,661,241-91,661,241 , GRCh38.p12 chr16: 76,837,141-76,837,141 , GRCh38.p12 chr3: 178,728,619-178,728,619 , GRCh38.p12 chr7: 117,134,799-117,134,799 , GRCh38.p12 chr16: 74,512,964-74,512,964 , GRCh38.p12 chr16: 74,512,955-74,512,955 , GRCh38.p12 chr2: 150,297,128-150,297,128 , GRCh38.p12 chr3: 178,728,632-178,728,632 , GRCh38.p12 chr16: 76,837,670-76,837,670 , GRCh38.p12 chr2: 150,297,104-150,297,104 , GRCh38.p12 chr7: 117,862,982-117,862,982 , GRCh38.p12 chr7: 118,001,458-118,001,458 , GRCh38.p12 chr8: 90,649,013-90,649,013 , GRCh38.p12 chr7: 117,134,813-117,134,813 , GRCh38.p12 chr7: 117,899,332-117,899,332 , GRCh38.p12 chr7: 117,951,137-117,951,137 , GRCh38.p12 chr8: 94,350,310-94,350,310 , GRCh38.p12 chr8: 94,350,318-94,350,318 , GRCh38.p12 chr7: 117,951,128-117,951,128 , GRCh38.p12 chr7: 118,001,455-118,001,455 , GRCh38.p12 chr8: 90,057,167-90,057,167 , GRCh38.p12 chr8: 90,057,176-90,057,176 , GRCh38.p12 chr8: 90,058,163-90,058,163 , GRCh38.p12 chr8: 89,293,552-89,293,552 , GRCh38.p12 chr8: 89,293,555-89,293,555 , GRCh38.p12 chr8: 90,058,426-90,058,426 , GRCh38.p12 chr8: 90,649,009-90,649,009 CALB1, GLG1, 7 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6246299mobile element insertion1nstd215human GRCh38 chr8: 90,068,670-90,068,670 , GRCh37.p13 chr8: 91,080,898-91,080,898 CALB1
    nsv6136610copy number variation1nstd213human GRCh37 chr8: 89,510,000-92,250,001 , GRCh38.p12 chr8: 88,497,771-91,237,773 LRRC69, COX6B1P6, 29 more genes
    nsv6136609copy number variation1nstd213human GRCh37 chr8: 87,900,000-91,530,001 , GRCh38.p12 chr8: 86,887,772-90,517,773 CALB1, RLIG1P3, 26 more genes
    nsv6136607copy number variation1nstd213human GRCh37 chr8: 87,430,000-94,700,001 , GRCh38.p12 chr8: 86,417,771-93,687,773 CALB1, WWP1, 73 more genes
    nsv6136605copy number variation1nstd213human GRCh37 chr8: 86,730,000-120,700,001 , GRCh38.p12 chr8: 85,717,771-119,687,761 CALB1, CDH17, 421 more genes
    nsv6136082copy number variation1nstd213human GRCh37 chr8: 86,730,000-142,740,001 , GRCh38.p12 chr8: 85,717,771-141,729,803 ANXA13, ATP6V1C1, 658 more genes
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