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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7098705complex chromosomal rearrangement16nstd230human GRCh37 chr6: 152,298,852-152,298,852 , GRCh37 chr6: 152,298,855-152,298,855 , GRCh37 chr6: 152,461,093-152,461,093 , GRCh37 chr6: 152,461,093-152,461,093 , GRCh37 chr6: 152,690,618-152,690,618 , GRCh37 chr6: 152,690,827-152,690,827 , GRCh37 chr6: 152,692,590-152,692,590 , GRCh37 chr6: 152,692,596-152,692,596 , GRCh37 chr6: 152,692,616-152,692,616 , GRCh37 chr6: 152,692,620-152,692,620 , GRCh37 chr6: 152,697,228-152,697,228 , GRCh37 chr6: 152,697,240-152,697,240 , GRCh37 chr6: 153,511,451-153,511,451 , GRCh37 chr6: 153,511,464-153,511,464 , GRCh37 chr6: 153,511,478-153,511,478 , GRCh37 chr6: 153,511,479-153,511,479 , GRCh37 chr6: 153,621,313-153,621,313 , GRCh37 chr6: 153,621,317-153,621,317 , GRCh37 chr6: 153,863,854-153,863,854 , GRCh37 chr6: 153,863,854-153,863,854 , GRCh37 chr13: 82,735,924-82,735,924 , GRCh37 chr13: 82,735,928-82,735,928 , GRCh37 chr13: 87,918,047-87,918,047 , GRCh37 chr13: 87,918,061-87,918,061 , GRCh37 chr13: 107,614,717-107,614,717 , GRCh37 chr13: 107,614,717-107,614,717 , GRCh37 chr13: 107,657,183-107,657,183 , GRCh37 chr13: 107,657,185-107,657,185 , GRCh37 chr15: 98,510,600-98,510,600 , GRCh37 chr15: 98,510,601-98,510,601 , GRCh37 chr16: 26,210,170-26,210,170 , GRCh37 chr16: 26,210,189-26,210,189 , GRCh38.p12 chr15: 97,967,370-97,967,370 , GRCh38.p12 chr15: 97,967,371-97,967,371 , GRCh38.p12 chr16: 26,198,849-26,198,849 , GRCh38.p12 chr16: 26,198,868-26,198,868 , GRCh38.p12 chr6: 151,977,717-151,977,717 , GRCh38.p12 chr6: 151,977,720-151,977,720 , GRCh38.p12 chr6: 152,139,958-152,139,958 , GRCh38.p12 chr6: 152,139,958-152,139,958 , GRCh38.p12 chr6: 152,369,483-152,369,483 , GRCh38.p12 chr6: 152,369,692-152,369,692 , GRCh38.p12 chr6: 152,371,455-152,371,455 , GRCh38.p12 chr6: 152,371,461-152,371,461 , GRCh38.p12 chr6: 152,371,481-152,371,481 , GRCh38.p12 chr6: 152,371,485-152,371,485 , GRCh38.p12 chr6: 152,376,093-152,376,093 , GRCh38.p12 chr6: 152,376,105-152,376,105 , GRCh38.p12 chr6: 153,190,316-153,190,316 , GRCh38.p12 chr6: 153,190,329-153,190,329 , GRCh38.p12 chr6: 153,190,343-153,190,343 , GRCh38.p12 chr6: 153,190,344-153,190,344 , GRCh38.p12 chr6: 153,300,178-153,300,178 , GRCh38.p12 chr6: 153,300,182-153,300,182 , GRCh38.p12 chr6: 153,542,719-153,542,719 , GRCh38.p12 chr6: 153,542,719-153,542,719 , GRCh38.p12 chr13: 82,161,789-82,161,789 , GRCh38.p12 chr13: 82,161,793-82,161,793 , GRCh38.p12 chr13: 87,265,792-87,265,792 , GRCh38.p12 chr13: 87,265,806-87,265,806 , GRCh38.p12 chr13: 106,962,369-106,962,369 , GRCh38.p12 chr13: 106,962,369-106,962,369 , GRCh38.p12 chr13: 107,004,835-107,004,835 , GRCh38.p12 chr13: 107,004,837-107,004,837 ESR1, SYNE1, 1 more genes
    nsv7075857inversion1nstd229human GRCh38 chr15: 97,972,769-97,977,456 , GRCh37.p13 chr15: 98,515,999-98,520,686 ARRDC4
    nsv7071991inversion1nstd229human GRCh38 chr15: 97,646,915-98,873,098 , GRCh37.p13 chr15: 98,190,145-99,416,327 LOC105371010, IGF1R, 11 more genes
    nsv7071701inversion1nstd229human GRCh38 chr15: 97,401,958-99,036,668 , GRCh37.p13 chr15: 97,945,188-99,529,036 IGF1R, ARRDC4, 18 more genes
    nsv7064669inversion1nstd229human GRCh38 chr15: 97,926,036-98,552,749 , GRCh37.p13 chr15: 98,469,266-99,095,978 LINC01582, FAM169BP, 7 more genes
    nsv6977640copy number variation1nstd229human GRCh38 chr15: 97,941,516-98,572,763 , GRCh37.p13 chr15: 98,484,746-99,115,992 RNU6-1186P, LOC105371009, 7 more genes
    nsv6973396copy number variation1nstd229human GRCh38 chr15: 97,172,326-98,354,236 , GRCh37.p13 chr15: 97,715,556-98,897,465 LOC105371007, LOC105371010, 13 more genes
    nsv6965315copy number variation1nstd229human GRCh38 chr15: 97,835,759-98,017,770 , GRCh37.p13 chr15: 98,378,989-98,561,000 LINC00923, LINC02251, 2 more genes
    nsv6962168copy number variation1nstd229human GRCh38 chr15: 97,968,653-97,994,793 , GRCh37.p13 chr15: 98,511,883-98,538,023 LOC105371009, ARRDC4
    nsv6960547copy number variation1nstd229human GRCh38 chr15: 93,794,809-100,070,222 , GRCh37.p13 chr15: 94,338,038-100,610,427 LOC105371010, LOC105371007, 81 more genes
    nsv6958298copy number variation1nstd229human GRCh38 chr15: 97,970,901-97,977,200 , GRCh37.p13 chr15: 98,514,131-98,520,430 ARRDC4
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6507657copy number variation1nstd223human GRCh38 chr15: 97,973,287-97,973,652 , GRCh37.p13 chr15: 98,516,517-98,516,882 ARRDC4
    nsv6505231copy number variation1nstd223human GRCh38 chr15: 97,958,501-97,963,900 , GRCh37.p13 chr15: 98,501,731-98,507,130 ARRDC4
    nsv6495716copy number variation1nstd223human GRCh38 chr15: 97,962,223-97,962,699 , GRCh37.p13 chr15: 98,505,453-98,505,929 ARRDC4
    nsv6314152copy number variation1nstd102humanPathogenic GRCh37 chr15: 97,026,327-102,429,112 , GRCh38.p12 chr15: 96,483,097-101,888,909 PCSK6, ASB7, 92 more genes
    nsv6313944copy number variation1nstd102humanPathogenic GRCh37 chr15: 94,836,128-101,302,111 , GRCh38.p12 chr15: 94,292,899-100,761,906 LINC01582, LRRC28, 85 more genes
    nsv6133155copy number variation1nstd213human GRCh37 chr15: 72,730,000-102,440,001 , GRCh38.p12 chr15: 72,437,659-101,899,798 , BLM, 609 more genes
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