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Items: 1 to 20 of 198

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3157895copy number variation2nstd151human GRCh37 (hg19) chr7: 148,080,738-148,112,713 , GRCh38 (hg38) chr7|NT_187564.1: 165,308-199,216 , GRCh38 (hg38) chr7: 148,383,646-148,415,621 CNTNAP2
    nsv3142908copy number variation1nstd151human GRCh37 (hg19) chr7: 148,106,480-148,112,713 , GRCh38 (hg38) chr7|NT_187564.1: 193,167-199,216 , GRCh38 (hg38) chr7: 148,409,388-148,415,621 CNTNAP2
    nsv3115709copy number variation1nstd145human GRCh37 (hg19) chr7: 147,934,997-147,938,929 , GRCh38 (hg38) chr7|NT_187564.1: 23,032-26,964 , GRCh38 (hg38) chr7: 148,237,905-148,241,837 CNTNAP2
    nsv3109752copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr7: 147,986,528-148,232,245 , GRCh38 (hg38) chr7|NT_187564.1: 74,563-271,455 , GRCh38 (hg38) chr7: 148,289,436-148,535,153 , NCBI36 (hg18) chr7: 147,617,461-147,863,178 CNTNAP2
    nsv3088766mobile element insertion1nstd144human GRCh37 (hg19) chr7: 147,987,361-147,987,361 , GRCh38 (hg38) chr7|NT_187564.1: 75,396-75,396 , GRCh38 (hg38) chr7: 148,290,269-148,290,269 CNTNAP2
    nsv3088448mobile element insertion1nstd144human GRCh37 (hg19) chr7: 148,178,646-148,178,646 , GRCh38 (hg38) chr7: 148,481,554-148,481,554 , GRCh38 (hg38) chr7|NT_187564.1: 265,149-265,149 0
    nsv3088446mobile element insertion1nstd144human GRCh37 (hg19) chr7: 147,919,513-147,919,513 , GRCh38 (hg38) chr7: 148,222,421-148,222,421 , GRCh38 (hg38) chr7|NT_187564.1: 7,548-7,548 CNTNAP2
    nsv3068734insertion1nstd90human GRCh37 (hg19) chr7: 148,028,874-148,028,874 , GRCh38 (hg38) chr7: 148,331,782-148,331,782 , GRCh38 (hg38) chr7|NT_187564.1: 116,909-116,909 CNTNAP2
    nsv2770961copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr7: 147,731,177-148,189,741 , GRCh38 (hg38) chr7: 148,034,085-148,492,649 , GRCh38 (hg38) chr7|NT_187564.1: 1-271,455 , NCBI36 (hg18) chr7: 147,362,110-147,820,674 CNTNAP2
    nsv2768363copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr7: 148,077,942-148,097,501 , GRCh38 (hg38) chr7|NT_187564.1: 162,514-182,058 , GRCh38 (hg38) chr7: 148,380,850-148,400,409 , NCBI36 (hg18) chr7: 147,708,875-147,728,434 CNTNAP2
    esv3851815copy number variation2estd219human GRCh37 (hg19) chr7: 148,091,051-148,094,452 , GRCh38 (hg38) chr7|NT_187564.1: 175,607-179,009 , GRCh38 (hg38) chr7: 148,393,959-148,397,360 CNTNAP2
    esv3851813copy number variation1270estd219human GRCh37 (hg19) chr7: 148,063,002-148,063,081 , GRCh38 (hg38) chr7: 148,365,910-148,365,989 , GRCh38 (hg38) chr7|NT_187564.1: 151,037-151,116 CNTNAP2
    esv3851811copy number variation1estd219human GRCh37 (hg19) chr7: 147,956,164-147,956,343 , GRCh38 (hg38) chr7: 148,259,072-148,259,251 , GRCh38 (hg38) chr7|NT_187564.1: 44,199-44,378 CNTNAP2
    esv3851812copy number variation2estd219human GRCh37 (hg19) chr7: 148,057,032-148,059,163 , GRCh38 (hg38) chr7|NT_187564.1: 145,067-147,198 , GRCh38 (hg38) chr7: 148,359,940-148,362,071 CNTNAP2
    esv3851810mobile element insertion2estd219human GRCh37 (hg19) chr7: 147,919,595-147,919,595 , GRCh38 (hg38) chr7|NT_187564.1: 7,630-7,630 , GRCh38 (hg38) chr7: 148,222,503-148,222,503 CNTNAP2
    esv3851816mobile element insertion85estd219human GRCh37 (hg19) chr7: 148,178,646-148,178,646 , GRCh38 (hg38) chr7|NT_187564.1: 265,149-265,149 , GRCh38 (hg38) chr7: 148,481,554-148,481,554 0
    esv3974873copy number variation1estd229human GRCh37 (hg19) chr7: 148,027,051-148,029,300 , GRCh38 (hg38) chr7|NT_187564.1: 115,086-117,335 , GRCh38 (hg38) chr7: 148,329,959-148,332,208 CNTNAP2
    esv3974871copy number variation1estd229human GRCh37 (hg19) chr7: 148,027,051-148,029,300 , GRCh38 (hg38) chr7: 148,329,959-148,332,208 , GRCh38 (hg38) chr7|NT_187564.1: 115,086-117,335 CNTNAP2
    esv3981995copy number variation1estd229human GRCh37 (hg19) chr7: 147,981,151-147,990,720 , GRCh38 (hg38) chr7: 148,284,059-148,293,628 , GRCh38 (hg38) chr7|NT_187564.1: 69,186-78,755 CNTNAP2
    nsv2745978copy number variation1nstd130human NCBI36 (hg18) chr7: 147,700,415-147,715,565 , GRCh37 (hg19) chr7: 148,069,482-148,084,632 , GRCh38 (hg38) chr7: 148,372,390-148,387,540 , GRCh38 (hg38) chr7|NT_187564.1: 157,517-169,192 CNTNAP2
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