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Items: 1 to 20 of 589

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2773586copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr14: 91,244,289-91,454,541 , GRCh37 (hg19) chr14: 92,174,536-92,384,788 , GRCh38 (hg38) chr14: 91,708,192-91,854,371 , GRCh38 (hg38) chr14|NT_187598.1: 175,987-322,166 TC2N, CATSPERB
    esv3873931mobile element insertion68estd219human GRCh37 (hg19) chr14: 92,247,261-92,247,261 , GRCh38 (hg38) chr14: 91,780,917-91,780,917 , GRCh38 (hg38) chr14|NT_187598.1: 248,712-248,712 TC2N
    esv3873927mobile element insertion540estd219human GRCh37 (hg19) chr14: 92,116,020-92,116,020 , GRCh38 (hg38) chr14: 91,649,676-91,649,676 , GRCh38 (hg38) chr14|NT_187598.1: 117,471-117,471 CATSPERB
    esv3873929copy number variation1estd219human GRCh37 (hg19) chr14: 92,184,192-92,333,818 , GRCh38 (hg38) chr14: 91,717,848-91,854,371 , GRCh38 (hg38) chr14|NT_187598.1: 185,643-322,166 TC2N, CATSPERB
    esv3873930copy number variation1estd219human GRCh37 (hg19) chr14: 92,220,041-92,227,659 , GRCh38 (hg38) chr14|NT_187598.1: 221,492-229,110 , GRCh38 (hg38) chr14: 91,753,697-91,761,315 0
    esv3873928mobile element insertion2201estd219human GRCh37 (hg19) chr14: 92,125,068-92,125,068 , GRCh38 (hg38) chr14: 91,658,724-91,658,724 , GRCh38 (hg38) chr14|NT_187598.1: 126,519-126,519 CATSPERB
    nsv1775241short tandem repeat2nstd128human GRCh37 (hg19) chr14: 92,319,078-92,319,096 , GRCh38 (hg38) chr14: 91,852,734-91,852,752 , GRCh38 (hg38) chr14|NT_187598.1: 320,529-320,547 TC2N
    nsv1775240short tandem repeat2nstd128human GRCh37 (hg19) chr14: 92,300,804-92,300,822 , GRCh38 (hg38) chr14: 91,834,460-91,834,478 , GRCh38 (hg38) chr14|NT_187598.1: 302,255-302,273 TC2N
    nsv1775239short tandem repeat4nstd128human GRCh37 (hg19) chr14: 92,298,735-92,298,748 , GRCh38 (hg38) chr14|NT_187598.1: 300,186-300,199 , GRCh38 (hg38) chr14: 91,832,391-91,832,404 TC2N
    nsv1775238short tandem repeat4nstd128human GRCh37 (hg19) chr14: 92,295,396-92,295,410 , GRCh38 (hg38) chr14: 91,829,052-91,829,066 , GRCh38 (hg38) chr14|NT_187598.1: 296,847-296,861 TC2N
    nsv1775237short tandem repeat2nstd128human GRCh37 (hg19) chr14: 92,294,796-92,294,827 , GRCh38 (hg38) chr14|NT_187598.1: 296,247-296,278 , GRCh38 (hg38) chr14: 91,828,452-91,828,483 TC2N
    nsv1775236short tandem repeat2nstd128human GRCh37 (hg19) chr14: 92,286,890-92,286,901 , GRCh38 (hg38) chr14: 91,820,546-91,820,557 , GRCh38 (hg38) chr14|NT_187598.1: 288,341-288,352 TC2N
    nsv1775235short tandem repeat3nstd128human GRCh37 (hg19) chr14: 92,280,702-92,280,714 , GRCh38 (hg38) chr14: 91,814,358-91,814,370 , GRCh38 (hg38) chr14|NT_187598.1: 282,153-282,165 TC2N
    nsv1775234short tandem repeat2nstd128human GRCh37 (hg19) chr14: 92,278,342-92,278,352 , GRCh38 (hg38) chr14: 91,811,998-91,812,008 , GRCh38 (hg38) chr14|NT_187598.1: 279,793-279,803 TC2N
    nsv1775233short tandem repeat1nstd128human GRCh37 (hg19) chr14: 92,272,163-92,272,189 , GRCh38 (hg38) chr14: 91,805,819-91,805,845 , GRCh38 (hg38) chr14|NT_187598.1: 273,614-273,640 TC2N
    nsv1775232short tandem repeat2nstd128human GRCh37 (hg19) chr14: 92,267,286-92,267,298 , GRCh38 (hg38) chr14: 91,800,942-91,800,954 , GRCh38 (hg38) chr14|NT_187598.1: 268,737-268,749 TC2N
    nsv1775231short tandem repeat1nstd128human GRCh37 (hg19) chr14: 92,262,582-92,262,650 , GRCh38 (hg38) chr14|NT_187598.1: 264,033-264,101 , GRCh38 (hg38) chr14: 91,796,238-91,796,306 TC2N
    nsv1775230short tandem repeat3nstd128human GRCh37 (hg19) chr14: 92,258,102-92,258,112 , GRCh38 (hg38) chr14: 91,791,758-91,791,768 , GRCh38 (hg38) chr14|NT_187598.1: 259,553-259,563 TC2N
    nsv1775229short tandem repeat4nstd128human GRCh37 (hg19) chr14: 92,255,955-92,255,979 , GRCh38 (hg38) chr14: 91,789,611-91,789,635 , GRCh38 (hg38) chr14|NT_187598.1: 257,406-257,430 TC2N
    nsv1775228short tandem repeat4nstd128human GRCh37 (hg19) chr14: 92,255,774-92,255,805 , GRCh38 (hg38) chr14: 91,789,430-91,789,461 , GRCh38 (hg38) chr14|NT_187598.1: 257,225-257,256 TC2N
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