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Items: 1 to 20 of 218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099240copy number variation1nstd231human GRCh38.p12 chr1: 159,722,599-161,418,916 , GRCh37 chr1: 159,692,389-161,388,706 APOA2, ATP1A2, 87 more genes
    nsv7042802inversion1nstd229human GRCh38 chr1: 159,324,839-163,640,188 , GRCh37.p13 chr1: 159,294,629-163,609,919 TRG-GCC2-1, LOC107985220, 178 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
    nsv6643151copy number variation1nstd229human GRCh38 chr1: 161,056,580-161,363,232 , GRCh37.p13 chr1: 161,026,370-161,333,022 NR1I3, FCER1G, 23 more genes
    nsv6636729copy number variation1nstd102humanUncertain significance GRCh37 chr1: 160,778,879-161,190,622 , GRCh38.p12 chr1: 160,809,089-161,220,832 CD244, LOC646347, 24 more genes
    nsv6543080inversion1nstd223human GRCh38 chr1: 161,062,458-161,062,728 , GRCh37.p13 chr1: 161,032,248-161,032,518 ARHGAP30
    nsv6541483inversion1nstd223human GRCh38 chr1: 161,061,448-161,061,951 , GRCh37.p13 chr1: 161,031,238-161,031,741 ARHGAP30
    nsv6332269copy number variation1nstd223human GRCh38 chr1: 160,388,767-162,811,116 , GRCh37.p13 chr1: 160,358,557-162,780,906 ATF6-DT, RPS23P10, 119 more genes
    nsv6328487copy number variation1nstd223human GRCh38 chr1: 161,061,412-161,065,235 , GRCh37.p13 chr1: 161,031,202-161,035,025 ARHGAP30
    nsv6321256copy number variation1nstd223human GRCh38 chr1: 161,064,631-161,082,202 , GRCh37.p13 chr1: 161,034,421-161,051,992 NECTIN4-AS1, ARHGAP30, 1 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
    nsv6310595copy number variation2nstd102humanUncertain significance GRCh37 chr1: 158,581,054-162,750,036 , GRCh38.p12 chr1: 158,611,264-162,780,246 IGSF8, SETP9, 193 more genes
    nsv6290394copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 160,859,558-161,409,185 , GRCh38.p12 chr1: 160,889,768-161,439,395 APOA2, FCER1G, 39 more genes
    nsv6245324mobile element insertion1nstd215human GRCh38 chr1: 161,055,886-161,055,886 , GRCh37.p13 chr1: 161,025,676-161,025,676 ARHGAP30
    nsv6163418copy number variation1nstd214human GRCh38 chr1: 161,055,883-161,055,934 , GRCh37.p13 chr1: 161,025,673-161,025,724 ARHGAP30
    nsv6133743copy number variation1nstd213human GRCh37 chr1: 160,920,000-161,500,001 , GRCh38.p12 chr1: 160,950,210-161,530,211 HSPA6, NIT1, 67 more genes
    nsv6133742copy number variation1nstd213human GRCh37 chr1: 158,430,000-161,510,001 , GRCh38.p12 chr1: 158,460,210-161,540,211 APCS, FCER1A, 174 more genes
    nsv6133741copy number variation1nstd213human GRCh37 chr1: 158,390,000-161,480,001 , GRCh38.p12 chr1: 158,420,210-161,510,211 ATP1A4, CD48, 169 more genes
    nsv6133740copy number variation1nstd213human GRCh37 chr1: 158,330,000-161,530,001 , GRCh38.p12 chr1: 158,360,210-161,560,211 ATP1A2, ATP1A4, 178 more genes
    nsv6050458insertion1nstd212human GRCh38 chr1: 161,061,385-161,061,385 , GRCh37.p13 chr1: 161,031,175-161,031,175 ARHGAP30
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