runx1t1[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3903985	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 92,378,841-93,053,423 , GRCh38.p12 chr8: 91,366,613-92,041,195	RUNX1T1, PRR13P7, 3 more genes
nsv3911034	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 79,584,698-96,379,096 , NCBI36 chr8: 79,747,253-96,448,272 , GRCh38 chr8: 78,672,463-95,366,868	RUNX1T1, LOC105375933, 233 more genes
nsv7137123	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 89,179,899-97,978,274 , GRCh38.p12 chr8: 88,167,670-96,966,046	RUNX1T1, SLC26A7, 112 more genes
nsv3912913	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 92,022,400-95,619,747 , GRCh37 chr8: 91,953,224-95,550,571 , GRCh38 chr8: 90,940,996-94,538,343	RUNX1T1, LOC101926956, 51 more genes
nsv3915173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636	RUNX1T1, RN7SL474P, 2109 more genes
nsv3901821	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028	RUNX1T1, TBC1D31, 2109 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	RUNX1T1, LOC101929488, 2105 more genes
nsv3916777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575	RUNX1T1, RPL5P22, 2105 more genes
nsv3898123	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385	RUNX1T1, SPAG1, 2105 more genes
nsv3908608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028	RUNX1T1, LINC01617, 2105 more genes
nsv3893757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442	RUNX1T1, LOC105375890, 2105 more genes
nsv3923310	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098	RUNX1T1, LOC112268023, 2105 more genes
nsv3914307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,605-146,280,167 , GRCh38 chr8: 241,605-145,054,781 , NCBI36 chr8: 181,605-146,250,971	RUNX1T1, LOC107986897, 2104 more genes
nsv3919282	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824	RUNX1T1, MIR4662B, 2104 more genes
nsv3919200	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639	RUNX1T1, LOC112268023, 2103 more genes
nsv3906425	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 12,490,999-146,295,771 , GRCh38.p12 chr8: 12,633,490-145,070,385	RUNX1T1, LOC112268016, 1819 more genes
nsv3915762	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 21,193,313-146,266,575 , GRCh38 chr8: 21,291,522-145,070,385 , GRCh37 chr8: 21,149,033-146,295,771	RUNX1T1, LOC105375693, 1718 more genes
nsv4456811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385	RUNX1T1, TERF1, 1511 more genes
nsv3916438	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 46,942,962-140,297,737 , NCBI36 chr8: 47,062,127-140,366,919 , GRCh38 chr8: 46,031,340-139,285,494	RUNX1T1, NDUFS5P6, 1152 more genes
nsv6634360	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385	RUNX1T1, WASHC5, 1028 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 34

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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