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Items: 1 to 20 of 341

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129787insertion1nstd186human GRCh37 chr17: 75,280,171-75,280,173 , GRCh38.p12 chr17: 77,284,089-77,284,091 , GRCh38.p12 chr17|NW_003315955.1: 74,982-74,984 LOC107984143, SEPTIN9
    nsv5382082mobile element deletion2nstd186human GRCh37 chr17: 75,235,964-75,236,290 , GRCh38.p12 chr17: 77,239,882-77,240,208 , GRCh38.p12 chr17|NW_003315955.1: 30,775-31,099 0
    nsv5337614translocation1nstd200human GRCh37 chr17: 75,245,988-75,245,988 , GRCh37 chr17: 75,245,876-75,245,876 , GRCh38.p12 chr17: 77,249,794-77,249,794 , GRCh38.p12 chr17: 77,249,906-77,249,906 , GRCh38.p12 chr17|NW_003315955.1: 40,687-40,687 , GRCh38.p12 chr17|NW_003315955.1: 40,799-40,799 0
    nsv5334931translocation1nstd200human GRCh37 chr17: 75,281,037-75,281,037 , GRCh37 chr17: 75,280,959-75,280,959 , GRCh38.p12 chr17|NW_003315955.1: 75,770-75,770 , GRCh38.p12 chr17|NW_003315955.1: 75,848-75,848 , GRCh38.p12 chr17: 77,284,877-77,284,877 , GRCh38.p12 chr17: 77,284,955-77,284,955 SEPTIN9, LOC107984143
    nsv4859077copy number variation1nstd200human GRCh37 chr17: 75,285,721-75,289,924 , GRCh38.p12 chr17|NW_003315955.1: 80,532-84,735 , GRCh38.p12 chr17: 77,289,639-77,293,842 SEPTIN9, LOC107984143
    nsv4859076copy number variation1nstd200human GRCh37 chr17: 75,269,303-75,271,034 , GRCh38.p12 chr17|NW_003315955.1: 64,114-65,845 , GRCh38.p12 chr17: 77,273,221-77,274,952 LACAT1, SEPTIN9-DT
    nsv4859075copy number variation1nstd200human GRCh37 chr17: 75,264,031-75,273,218 , GRCh38.p12 chr17: 77,267,949-77,277,136 , GRCh38.p12 chr17|NW_003315955.1: 58,842-68,029 LACAT1, SEPTIN9-DT
    nsv4859074copy number variation1nstd200human GRCh37 chr17: 75,246,547-75,247,513 , GRCh38.p12 chr17|NW_003315955.1: 41,358-42,324 , GRCh38.p12 chr17: 77,250,465-77,251,431 0
    nsv4859073copy number variation1nstd200human GRCh37 chr17: 75,246,212-75,247,388 , GRCh38.p12 chr17: 77,250,130-77,251,306 , GRCh38.p12 chr17|NW_003315955.1: 41,023-42,199 0
    nsv4859072copy number variation1nstd200human GRCh37 chr17: 75,242,055-75,242,208 , GRCh38.p12 chr17|NW_003315955.1: 36,866-37,019 , GRCh38.p12 chr17: 77,245,973-77,246,126 0
    nsv4859070copy number variation1nstd200human GRCh37 chr17: 75,218,378-75,218,886 , GRCh38.p12 chr17: 77,222,296-77,222,804 , GRCh38.p12 chr17|NW_003315955.1: 13,184-13,692 0
    nsv4769570mobile element deletion1nstd200human GRCh37 chr17: 75,287,118-75,287,412 , GRCh38.p12 chr17|NW_003315955.1: 81,929-82,223 , GRCh38.p12 chr17: 77,291,036-77,291,330 LOC107984143, SEPTIN9
    nsv4769569mobile element deletion1nstd200human GRCh37 chr17: 75,258,888-75,259,222 , GRCh38.p12 chr17|NW_003315955.1: 53,699-54,033 , GRCh38.p12 chr17: 77,262,806-77,263,140 LACAT1
    nsv4769568mobile element deletion1nstd200human GRCh37 chr17: 75,235,964-75,236,290 , GRCh38.p12 chr17: 77,239,882-77,240,208 , GRCh38.p12 chr17|NW_003315955.1: 30,775-31,099 0
    nsv4739488copy number variation1nstd199human GRCh37 chr17: 75,245,858-75,245,943 , GRCh38.p12 chr17: 77,249,776-77,249,861 , GRCh38.p12 chr17|NW_003315955.1: 40,669-40,754 0
    nsv4735428copy number variation1nstd199human GRCh37 chr17: 75,242,050-75,242,217 , GRCh38.p12 chr17|NW_003315955.1: 36,861-37,028 , GRCh38.p12 chr17: 77,245,968-77,246,135 0
    nsv4734106copy number variation1nstd199human GRCh37 chr17: 75,235,960-75,236,302 , GRCh38.p12 chr17: 77,239,878-77,240,220 , GRCh38.p12 chr17|NW_003315955.1: 30,771-31,111 0
    nsv4706130copy number variation3nstd195human GRCh37 chr17: 75,235,948-75,235,949 , GRCh38.p12 chr17: 77,239,866-77,239,867 , GRCh38.p12 chr17|NW_003315955.1: 30,759-30,760 0
    nsv4667628copy number variation1nstd186human GRCh37 chr17: 75,263,903-75,273,169 , GRCh38.p12 chr17|NW_003315955.1: 58,714-67,980 , GRCh38.p12 chr17: 77,267,821-77,277,087 LACAT1, SEPTIN9-DT
    nsv4639886copy number variation2nstd186human GRCh37 chr17: 75,235,964-75,236,290 , GRCh38.p12 chr17|NW_003315955.1: 30,775-31,099 , GRCh38.p12 chr17: 77,239,882-77,240,208 0
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