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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097684copy number variation1nstd102humanUncertain significance GRCh37 chr9: 124,062,140-124,091,613 , GRCh38.p12 chr9: 121,299,862-121,329,335 GSN
    nsv6877727copy number variation1nstd229human GRCh38 chr9: 121,242,877-121,243,005 , GRCh37.p13 chr9: 124,005,155-124,005,283 GSN
    nsv6877171copy number variation1nstd229human GRCh38 chr9: 121,224,023-121,224,063 , GRCh37.p13 chr9: 123,986,301-123,986,341 GSN
    nsv6875616copy number variation1nstd229human GRCh38 chr9: 121,268,701-121,321,400 , GRCh37.p13 chr9: 124,030,979-124,083,678 GSN-AS1, GSN
    nsv6874653copy number variation1nstd229human GRCh38 chr9: 121,329,317-121,331,383 , GRCh37.p13 chr9: 124,091,595-124,093,661 GSN
    nsv6872256copy number variation1nstd229human GRCh38 chr9: 121,237,547-121,247,897 , GRCh37.p13 chr9: 123,999,825-124,010,175 GSN, LOC645482
    nsv6872101copy number variation1nstd229human GRCh38 chr9: 121,314,025-121,317,083 , GRCh37.p13 chr9: 124,076,303-124,079,361 GSN
    nsv6870753copy number variation1nstd229human GRCh38 chr9: 121,243,161-121,300,982 , GRCh37.p13 chr9: 124,005,439-124,063,260 GSN-AS1, GSN
    nsv6866182copy number variation1nstd229human GRCh38 chr9: 121,318,880-121,321,267 , GRCh37.p13 chr9: 124,081,158-124,083,545 GSN
    nsv6865276copy number variation1nstd229human GRCh38 chr9: 121,286,039-121,366,075 , GRCh37.p13 chr9: 124,048,317-124,128,353 GSN, STOM
    nsv6864957copy number variation1nstd229human GRCh38 chr9: 121,326,448-121,326,537 , GRCh37.p13 chr9: 124,088,726-124,088,815 GSN
    nsv6864121copy number variation1nstd229human GRCh38 chr9: 121,281,562-121,301,960 , GRCh37.p13 chr9: 124,043,840-124,064,238 GSN-AS1, GSN
    nsv6864062copy number variation1nstd229human GRCh38 chr9: 121,267,287-121,268,828 , GRCh37.p13 chr9: 124,029,565-124,031,106 GSN
    nsv6863827copy number variation1nstd229human GRCh38 chr9: 121,327,716-121,327,851 , GRCh37.p13 chr9: 124,089,994-124,090,129 GSN
    nsv6862737copy number variation1nstd229human GRCh38 chr9: 121,289,716-121,293,857 , GRCh37.p13 chr9: 124,051,994-124,056,135 GSN
    nsv6862685copy number variation1nstd229human GRCh38 chr9: 121,303,063-121,310,681 , GRCh37.p13 chr9: 124,065,341-124,072,959 GSN
    nsv6860580copy number variation1nstd229human GRCh38 chr9: 121,253,488-121,755,032 , GRCh37.p13 chr9: 124,015,766-124,517,311 RN7SL187P, GGTA1, 8 more genes
    nsv6859094copy number variation1nstd229human GRCh38 chr9: 121,322,458-121,328,066 , GRCh37.p13 chr9: 124,084,736-124,090,344 GSN
    nsv6858984copy number variation1nstd229human GRCh38 chr9: 121,279,653-121,282,197 , GRCh37.p13 chr9: 124,041,931-124,044,475 GSN-AS1, GSN
    nsv6858121copy number variation1nstd229human GRCh38 chr9: 121,202,166-121,210,125 , GRCh37.p13 chr9: 123,964,444-123,972,403 RAB14, GSN, 1 more genes
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