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Items: 1 to 20 of 201

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7077533inversion1nstd229human GRCh38 chr8: 125,245,829-133,039,076 , GRCh37.p13 chr8: 126,258,071-134,051,321 PVT1, MTRF1LP2, 76 more genes
    nsv7075754inversion1nstd229human GRCh38 chr8: 126,056,701-127,370,200 , GRCh37.p13 chr8: 127,068,945-128,382,446 LRATD2, PCAT1, 15 more genes
    nsv6857318copy number variation1nstd229human GRCh38 chr8: 126,364,525-132,576,581 , GRCh37.p13 chr8: 127,376,770-133,588,829 PRNCR1, MIR1205, 59 more genes
    nsv6856000copy number variation1nstd229human GRCh38 chr8: 124,373,188-128,390,224 , GRCh37.p13 chr8: 125,385,429-129,402,470 WASHC5, MIR4662B, 57 more genes
    nsv6853512copy number variation1nstd229human GRCh38 chr8: 126,547,401-126,551,300 , GRCh37.p13 chr8: 127,559,646-127,563,545 LRATD2
    nsv6852752copy number variation1nstd229human GRCh38 chr8: 126,558,479-126,562,930 , GRCh37.p13 chr8: 127,570,724-127,575,175 LOC105375751, LRATD2
    nsv6848939copy number variation1nstd229human GRCh38 chr8: 126,544,429-126,555,459 , GRCh37.p13 chr8: 127,556,674-127,567,704 LOC105375751, LRATD2
    nsv6841023copy number variation1nstd229human GRCh38 chr8: 126,514,101-126,602,507 , GRCh37.p13 chr8: 127,526,346-127,614,752 LOC105375751, LRATD2, 1 more genes
    nsv6838710copy number variation1nstd229human GRCh38 chr8: 126,440,001-126,604,300 , GRCh37.p13 chr8: 127,452,246-127,616,545 LRATD2, LOC105375750, 2 more genes
    nsv6637224copy number variation1nstd102humanPathogenic GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133 RNU4-37P, LOC100420215, 220 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6305143copy number variation1nstd186human GRCh37 chr8: 127,559,612-127,563,541 , GRCh38.p12 chr8: 126,547,367-126,551,296 LRATD2
    nsv6290936copy number variation1nstd102humanUncertain significance GRCh37 chr8: 127,511,861-128,100,345 , GRCh38.p12 chr8: 126,499,616-127,088,100 PCAT2, RNU11-4P, 8 more genes
    nsv6136309copy number variation1nstd213human GRCh37 chr8: 122,920,000-127,650,001 , GRCh38.p12 chr8: 121,907,761-126,637,756 TBC1D31, FAM91A1, 77 more genes
    nsv6136245copy number variation1nstd213human GRCh37 chr8: 127,180,000-127,910,001 , GRCh38.p12 chr8: 126,167,756-126,897,756 LRATD2, RFPL4AP5, 6 more genes
    nsv6136082copy number variation1nstd213human GRCh37 chr8: 86,730,000-142,740,001 , GRCh38.p12 chr8: 85,717,771-141,729,803 ANXA13, ATP6V1C1, 658 more genes
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