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Items: 1 to 20 of 260

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3137212copy number variation1nstd151human GRCh37 (hg19) chr5: 1,052,472-1,076,932 , GRCh38.p2 chr5|NT_187548.1: 70,866-94,644 , GRCh38 (hg38) chr5: 1,052,357-1,076,817 SLC12A7, MIR4635
    nsv3137045copy number variation1nstd151human GRCh37 (hg19) chr5: 1,032,264-1,282,744 , GRCh38 (hg38) chr5: 1,032,149-1,282,629 , GRCh38.p2 chr5|NT_187548.1: 50,656-179,043 TERT, SLC12A7, 7 more genes
    nsv3136483copy number variation2nstd151human GRCh37 (hg19) chr5: 1,057,583-1,060,571 , GRCh38.p2 chr5|NT_187548.1: 75,977-78,973 , GRCh38 (hg38) chr5: 1,057,468-1,060,456 SLC12A7
    nsv3134409copy number variation1nstd151human GRCh37 (hg19) chr5: 1,052,472-1,094,368 , GRCh38.p2 chr5|NT_187548.1: 70,866-111,935 , GRCh38 (hg38) chr5: 1,052,357-1,094,253 SLC12A7, MIR4635
    nsv3133862copy number variation1nstd151human GRCh37 (hg19) chr5: 1,088,418-1,213,693 , GRCh38 (hg38) chr5: 1,088,303-1,213,578 , GRCh38.p2 chr5|NT_187548.1: 105,985-179,043 SLC12A7, SLC6A19, 3 more genes
    nsv3131740copy number variation4nstd151human GRCh37 (hg19) chr5: 1,032,264-1,094,368 , GRCh38 (hg38) chr5: 1,032,149-1,094,253 , GRCh38.p2 chr5|NT_187548.1: 50,656-111,935 SLC12A7, NKD2, 1 more genes
    nsv3131098copy number variation4nstd151human GRCh37 (hg19) chr5: 1,032,264-1,233,008 , GRCh38.p2 chr5|NT_187548.1: 50,656-179,043 , GRCh38 (hg38) chr5: 1,032,149-1,232,893 NKD2, SLC6A19, 6 more genes
    nsv3130854copy number variation1nstd151human GRCh37 (hg19) chr5: 1,033,484-1,036,504 , GRCh38.p2 chr5|NT_187548.1: 51,876-54,896 , GRCh38 (hg38) chr5: 1,033,369-1,036,389 NKD2
    nsv3130211copy number variation1nstd151human GRCh37 (hg19) chr5: 1,052,320-1,060,571 , GRCh38 (hg38) chr5: 1,052,205-1,060,456 , GRCh38.p2 chr5|NT_187548.1: 70,714-78,973 SLC12A7
    nsv3129723copy number variation1nstd151human GRCh37 (hg19) chr5: 1,034,347-1,036,504 , GRCh38 (hg38) chr5: 1,034,232-1,036,389 , GRCh38.p2 chr5|NT_187548.1: 52,739-54,896 NKD2
    nsv3129515copy number variation1nstd151human GRCh37 (hg19) chr5: 1,032,264-1,087,153 , GRCh38.p2 chr5|NT_187548.1: 50,656-104,720 , GRCh38 (hg38) chr5: 1,032,149-1,087,038 SLC12A7, NKD2, 1 more genes
    nsv3128335copy number variation1nstd151human GRCh37 (hg19) chr5: 1,032,264-1,038,724 , GRCh38 (hg38) chr5: 1,032,149-1,038,609 , GRCh38.p2 chr5|NT_187548.1: 50,656-57,116 NKD2
    nsv3126301copy number variation1nstd151human GRCh37 (hg19) chr5: 1,032,264-1,089,248 , GRCh38 (hg38) chr5: 1,032,149-1,089,133 , GRCh38.p2 chr5|NT_187548.1: 50,656-106,815 NKD2, MIR4635, 1 more genes
    nsv3125871copy number variation1nstd151human GRCh37 (hg19) chr5: 1,032,264-1,235,782 , GRCh38 (hg38) chr5: 1,032,149-1,235,667 , GRCh38.p2 chr5|NT_187548.1: 50,656-179,043 SLC12A7, NKD2, 6 more genes
    nsv3123658copy number variation1nstd151human GRCh37 (hg19) chr5: 1,079,510-1,094,368 , GRCh38 (hg38) chr5: 1,079,395-1,094,253 , GRCh38.p2 chr5|NT_187548.1: 97,224-111,935 SLC12A7
    nsv3119877copy number variation1nstd151human GRCh37 (hg19) chr5: 1,057,583-1,221,433 , GRCh38.p2 chr5|NT_187548.1: 75,977-179,043 , GRCh38 (hg38) chr5: 1,057,468-1,221,318 MIR4635, SLC6A19, 4 more genes
    nsv3119740copy number variation1nstd151human GRCh37 (hg19) chr5: 1,093,645-1,213,693 , GRCh38 (hg38) chr5: 1,093,530-1,213,578 , GRCh38.p2 chr5|NT_187548.1: 111,212-179,043 CTD-3080P12.3, LOC107986396, 3 more genes
    nsv3119412copy number variation2nstd151human GRCh37 (hg19) chr5: 1,073,745-1,094,368 , GRCh38 (hg38) chr5: 1,073,630-1,094,253 , GRCh38.p2 chr5|NT_187548.1: 91,457-111,935 SLC12A7
    nsv3111344copy number variation1nstd145human GRCh37 (hg19) chr5: 1,040,193-1,189,477 , GRCh38.p2 chr5|NT_187548.1: 58,585-179,043 , GRCh38 (hg38) chr5: 1,040,078-1,189,362 CTD-3080P12.3, LOC107986396, 3 more genes
    nsv3071165insertion1nstd90human GRCh37 (hg19) chr5: 1,070,127-1,070,128 , GRCh38 (hg38) chr5: 1,070,012-1,070,013 , GRCh38.p2 chr5|NT_187548.1: 88,151-88,152 SLC12A7
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