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Items: 1 to 20 of 140

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057537inversion1nstd229human GRCh38 chr1: 161,493,525-166,518,262 , GRCh37.p13 chr1: 161,463,315-166,487,499 LOC107985451, ALDH9A1, 88 more genes
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6643977copy number variation1nstd229human GRCh38 chr1: 165,769,767-165,783,379 , GRCh37.p13 chr1: 165,739,004-165,752,616 TMCO1-AS1
    nsv6643976copy number variation1nstd229human GRCh38 chr1: 165,731,562-165,793,595 , GRCh37.p13 chr1: 165,700,799-165,762,832 TMCO1-AS1, TMCO1
    nsv6643959copy number variation1nstd229human GRCh38 chr1: 165,255,035-165,794,434 , GRCh37.p13 chr1: 165,224,272-165,763,671 RPL21P27, LRRC52, 11 more genes
    nsv6643489copy number variation1nstd229human GRCh38 chr1: 165,771,926-165,784,191 , GRCh37.p13 chr1: 165,741,163-165,753,428 TMCO1-AS1
    nsv6547688inversion1nstd223human GRCh38 chr1: 165,771,476-165,772,093 , GRCh37.p13 chr1: 165,740,713-165,741,330 TMCO1-AS1
    nsv6540250inversion1nstd223human GRCh38 chr1: 163,441,141-169,028,378 , GRCh37.p13 chr1: 163,410,931-168,997,616 LOC107985452, NMNAT1P2, 96 more genes
    nsv6539985inversion1nstd223human GRCh38 chr1: 165,770,121-165,771,276 , GRCh37.p13 chr1: 165,739,358-165,740,513 TMCO1-AS1
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 LOC100420658, LOC105371610, 167 more genes
    nsv6313604copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,417,296-166,197,042 , GRCh38.p12 chr1: 160,447,506-166,227,805 USF1, TRE-CTC1-3, 161 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133594copy number variation1nstd213human GRCh37 chr1: 163,370,000-166,450,001 , GRCh38.p12 chr1: 163,400,210-166,480,764 PBX1, UCK2, 39 more genes
    nsv6133565copy number variation1nstd213human GRCh37 chr1: 164,310,000-170,640,001 , GRCh38.p12 chr1: 164,340,763-170,670,860 ATP1B1, DPT, 126 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5371481translocation1nstd200human GRCh38 chr1: 165,769,259-165,769,259 , GRCh38 chr1: 164,958,581-164,958,581 , GRCh37.p13 chr1: 164,927,818-164,927,818 , GRCh37.p13 chr1: 165,738,496-165,738,496 TMCO1-AS1, TMCO1
    nsv5332462translocation1nstd200human GRCh37 chr1: 164,927,818-164,927,818 , GRCh37 chr1: 165,738,496-165,738,496 , GRCh38.p12 chr1: 164,958,581-164,958,581 , GRCh38.p12 chr1: 165,769,259-165,769,259 TMCO1-AS1, TMCO1
    nsv5041452inversion1nstd200human GRCh38 chr1: 163,441,139-169,028,376 , GRCh37.p13 chr1: 163,410,929-168,997,614 , RPS17P6, 97 more genes
    nsv4897865copy number variation1nstd200human GRCh38 chr1: 165,769,258-165,771,239 , GRCh37.p13 chr1: 165,738,495-165,740,476 TMCO1-AS1, TMCO1
    nsv4784545copy number variation1nstd200human GRCh37 chr1: 165,738,495-165,740,476 , GRCh38.p12 chr1: 165,769,258-165,771,239 TMCO1, TMCO1-AS1
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