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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3920476copy number variation1nstd102humanLikely benign NCBI36 chr10: 47,010,385-47,172,593 , GRCh37.p13 chr10|NW_003871068.1: 440,258-589,544 , GRCh38 chr10: 46,169,143-46,331,351 ANTXRL, ANTXRLP1, 2 more genes
    nsv3885445copy number variation1nstd102humannot provided GRCh37 chr10: 47,543,322-47,703,869 , GRCh38.p12 chr10: 46,172,086-46,332,633 ANTXRL, AHCYP1, 2 more genes
    esv3648516copy number variation1estd216humannot provided GRCh38.p12 chr10: 46,172,086-46,332,633 , GRCh37 chr10: 47,543,322-47,703,869 ANTXRL, AHCYP1, 2 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 ANTXRL, RNU7-12P, 1876 more genes
    nsv4675455copy number variation1nstd102humanPathogenic GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325 ANTXRL, MRLN, 242 more genes
    nsv3919674copy number variation1nstd102humanPathogenic NCBI36 chr10: 49,100,986-52,085,077 , GRCh38 chr10: 45,931,517-50,655,311 , GRCh37 chr10: 49,430,980-52,415,071 ANTXRL, AGAP12P, 111 more genes
    nsv3911796copy number variation1nstd102humanPathogenic NCBI36 chr10: 45,525,696-51,581,091 , GRCh38 chr10: 45,710,242-50,151,325 , GRCh37 chr10: 46,205,690-51,911,085 ANTXRL, AGAP4, 111 more genes
    nsv3891326copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,225,364-51,874,356 , GRCh38.p12 chr10: 45,729,916-50,114,596 ANTXRL, AGAP9, 108 more genes
    nsv4455118copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,235,357-51,874,163 , GRCh38.p12 chr10: 45,739,909-50,114,403 ANTXRL, DUSP8P2, 108 more genes
    nsv7148121copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,284,269-51,870,080 , GRCh38.p12 chr10: 45,788,821-50,110,320 ANTXRL, LOC100420617, 108 more genes
    nsv3917908copy number variation1nstd102humanPathogenic GRCh38 chr10: 45,710,248-50,021,141 , GRCh37 chr10: 46,205,696-51,724,915 , NCBI36 chr10: 45,525,702-51,450,907 ANTXRL, LINC02675, 108 more genes
    nsv3896419copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,287,821-51,861,565 , GRCh38.p12 chr10: 45,792,373-50,101,805 ANTXRL, RHEBP1, 108 more genes
    nsv3917450copy number variation1nstd102humanPathogenic GRCh38 chr10: 45,710,242-49,929,364 , GRCh37 chr10: 46,205,690-51,330,432 , NCBI36 chr10: 45,525,696-51,265,056 ANTXRL, ANXA8L1, 102 more genes
    nsv3895921copy number variation2nstd102humanPathogenic GRCh37 chr10: 46,966,533-51,903,755 , GRCh38.p12 chr10: 45,931,517-50,143,995 ANTXRL, LINC02637, 104 more genes
    nsv3891496copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,224,446-51,594,991 , GRCh38.p12 chr10: 45,728,998-49,929,364 ANTXRL, ARHGAP22-IT1, 100 more genes
    nsv3904341copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,966,533-51,874,356 , GRCh38.p12 chr10: 45,931,517-50,114,596 ANTXRL, AGAP7P, 104 more genes
    nsv6634443copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,287,821-51,627,470 , GRCh38.p12 chr10: 45,792,373-49,929,364 ANTXRL, GLUD1P2, 100 more genes
    nsv4716588copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,964,973-51,826,226 , GRCh38.p12 chr10: 45,931,517-50,066,466 ANTXRL, MAPK8, 104 more genes
    nsv4350671copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,544,810-51,743,471 , GRCh38.p12 chr10: 45,931,517-49,983,711 ANTXRL, RNA5SP315, 100 more genes
    nsv6315547copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,576,515-51,680,164 , GRCh38.p12 chr10: 45,931,517-49,929,364 ANTXRL, ARHGAP22-IT1, 96 more genes
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