U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Nucleotide

Items: 1 to 20 of 965

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6307356copy number variation1nstd186human GRCh37 chr17: 44,775,346-44,781,346 , GRCh38.p12 chr17: 46,697,980-46,703,980 , GRCh38.p12 chr17|NT_187663.1: 1,217,407-1,223,405 , GRCh38.p12 chr17|NT_167251.2: 1,683,869-1,689,869 NSF, LRRC37A2
    nsv6307094copy number variation1nstd186human GRCh37 chr17: 44,763,346-44,779,346 , GRCh38.p12 chr17: 46,685,980-46,701,980 , GRCh38.p12 chr17|NT_187663.1: 1,205,403-1,221,405 , GRCh38.p12 chr17|NT_167251.2: 1,671,870-1,687,869 LRRC37A2, NSF
    nsv6113557copy number variation1nstd186human GRCh37 chr17: 44,775,346-44,780,466 , GRCh38.p12 chr17: 46,697,980-46,703,100 , GRCh38.p12 chr17|NT_187663.1: 1,217,407-1,222,525 , GRCh38.p12 chr17|NT_167251.2: 1,683,869-1,688,989 NSF, LRRC37A2
    nsv5336472translocation1nstd200human GRCh37 chr17: 44,868,607-44,868,607 , GRCh37 chr17: 44,874,249-44,874,249 , GRCh38.p12 chr17: 46,791,241-46,791,241 , GRCh38.p12 chr17|NT_187663.1: 1,316,303-1,316,303 , GRCh38.p12 chr17|NT_167251.2: 1,777,133-1,777,133 , GRCh38.p12 chr17|NT_167251.2: 1,782,776-1,782,776 , GRCh38.p12 chr17: 46,796,883-46,796,883 , GRCh38.p12 chr17|NT_187663.1: 1,310,658-1,310,658 WNT3, LRRC37A2
    nsv4769511mobile element deletion1nstd200human GRCh37 chr17: 44,785,887-44,786,190 , GRCh38.p12 chr17: 46,708,521-46,708,824 , GRCh38.p12 chr17|NT_187663.1: 1,227,947-1,228,250 , GRCh38.p12 chr17|NT_167251.2: 1,694,412-1,694,715 LRRC37A2, NSF
    nsv4640050copy number variation1nstd186human GRCh37 chr17: 44,726,700-44,738,200 , GRCh38.p12 chr17|NT_187663.1: 1,169,025-1,180,524 , GRCh38.p12 chr17: 46,649,334-46,660,834 , GRCh38.p12 chr17|NT_167251.2: 1,640,860-1,646,869 LRRC37A2, NSF
    nsv4636250copy number variation1nstd186human GRCh37 chr17: 44,888,182-44,888,655 , GRCh38.p12 chr17|NT_167251.2: 1,796,709-1,797,015 , GRCh38.p12 chr17: 46,810,816-46,811,289 , GRCh38.p12 chr17|NT_187663.1: 1,330,234-1,330,707 WNT3, LRRC37A2
    nsv4627843copy number variation1nstd183human GRCh37 chr17: 44,848,454-44,849,701 , GRCh38.p12 chr17|NT_187663.1: 1,290,500-1,291,742 , GRCh38.p12 chr17: 46,771,088-46,772,335 , GRCh38.p12 chr17|NT_167251.2: 1,756,967-1,758,209 WNT3, LRRC37A2
    nsv4621738copy number variation1nstd183human GRCh37 chr17: 44,805,973-44,806,441 , GRCh38.p12 chr17: 46,728,607-46,729,075 , GRCh38.p12 chr17|NT_187663.1: 1,248,036-1,248,504 , GRCh38.p12 chr17|NT_167251.2: 1,714,498-1,714,966 NSF, LRRC37A2
    nsv4557422mobile element insertion1nstd166human GRCh37.p13 chr17: 44,863,353-44,863,353 , GRCh38.p12 chr17|NT_187663.1: 1,305,398-1,305,398 , GRCh38.p12 chr17: 46,785,987-46,785,987 , GRCh38.p12 chr17|NT_167251.2: 1,771,873-1,771,873 LRRC37A2, WNT3
    nsv4531650copy number variation1nstd166human GRCh37.p13 chr17: 44,856,857-44,857,183 , GRCh38.p12 chr17: 46,779,491-46,779,817 , GRCh38.p12 chr17|NT_187663.1: 1,298,906-1,299,231 , GRCh38.p12 chr17|NT_167251.2: 1,765,377-1,765,703 LRRC37A2, WNT3
    nsv4514197mobile element insertion1nstd166human GRCh37.p13 chr17: 44,859,687-44,859,687 , GRCh38.p12 chr17: 46,782,321-46,782,321 , GRCh38.p12 chr17|NT_187663.1: 1,301,734-1,301,734 , GRCh38.p12 chr17|NT_167251.2: 1,768,207-1,768,207 WNT3, LRRC37A2
    nsv4500848mobile element insertion1nstd166human GRCh37.p13 chr17: 44,831,849-44,831,849 , GRCh38.p12 chr17: 46,754,483-46,754,483 , GRCh38.p12 chr17|NT_167251.2: 1,740,360-1,740,360 , GRCh38.p12 chr17|NT_187663.1: 1,273,894-1,273,894 NSF, LRRC37A2
    nsv4430447copy number variation1nstd174human GRCh37 chr17: 44,848,438-44,849,701 , GRCh38.p12 chr17|NT_167251.2: 1,756,951-1,758,209 , GRCh38.p12 chr17: 46,771,072-46,772,335 , GRCh38.p12 chr17|NT_187663.1: 1,290,484-1,291,742 LRRC37A2, WNT3
    nsv4423818copy number variation1nstd174human GRCh37 chr17: 44,637,378-44,834,833 , GRCh38.p12 chr17: 46,560,012-46,757,467 , GRCh38.p12 chr17|NT_187663.1: 1,079,714-1,276,879 , GRCh38.p12 chr17|NT_167251.2: 1,640,860-1,743,344 NSF, ARL17A, 4 more genes
    nsv4266697copy number variation1nstd166human GRCh37.p13 chr17: 44,786,208-44,786,975 , GRCh38.p12 chr17: 46,708,842-46,709,609 , GRCh38.p12 chr17|NT_187663.1: 1,228,270-1,229,037 , GRCh38.p12 chr17|NT_167251.2: 1,694,733-1,695,500 LRRC37A2, NSF
    nsv4263427copy number variation1nstd166human GRCh37.p13 chr17: 44,764,000-44,773,000 , GRCh38.p12 chr17: 46,686,634-46,695,634 , GRCh38.p12 chr17|NT_167251.2: 1,672,524-1,681,524 , GRCh38.p12 chr17|NT_187663.1: 1,206,057-1,215,061 LRRC37A2, NSF
    nsv4261832copy number variation1nstd166human GRCh37.p13 chr17: 44,765,000-44,784,000 , GRCh38.p12 chr17|NT_167251.2: 1,673,524-1,692,525 , GRCh38.p12 chr17: 46,687,634-46,706,634 , GRCh38.p12 chr17|NT_187663.1: 1,207,057-1,226,060 NSF, LRRC37A2
    nsv4259761copy number variation1nstd166human GRCh37.p13 chr17: 44,726,700-44,738,200 , GRCh38.p12 chr17|NT_187663.1: 1,169,025-1,180,524 , GRCh38.p12 chr17: 46,649,334-46,660,834 , GRCh38.p12 chr17|NT_167251.2: 1,640,860-1,646,869 LRRC37A2, NSF
    nsv4259327copy number variation1nstd166human GRCh37.p13 chr17: 44,845,299-44,845,401 , GRCh38.p12 chr17|NT_167251.2: 1,753,812-1,753,914 , GRCh38.p12 chr17: 46,767,933-46,768,035 , GRCh38.p12 chr17|NT_187663.1: 1,287,346-1,287,448 LRRC37A2, WNT3
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center