myct1[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3916405	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 150,744,068-159,894,974 , GRCh38 chr6: 150,381,239-159,553,952 , GRCh37 chr6: 150,702,375-159,974,984	MYCT1, LOC112267968, 126 more genes
nsv3920651	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 144,932,561-152,985,364 , NCBI36 chr6: 145,295,390-153,348,192 , GRCh37 chr6: 145,253,697-153,306,499	MYCT1, PPP1R14C, 107 more genes
nsv7148221	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958	MYCT1, RNU6-824P, 97 more genes
nsv4675234	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 149,431,322-154,120,064 , GRCh38.p12 chr6: 149,110,186-153,798,929	MYCT1, RNU7-3P, 86 more genes
nsv3882645	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 152,443,551-153,748,051 , GRCh38 chr6: 152,122,416-153,426,916	MYCT1, LOC107986661, 18 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	MYCT1, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	MYCT1, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	MYCT1, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	MYCT1, ITPR3, 2905 more genes
nsv3911993	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033	MYCT1, LOC105369171, 418 more genes
nsv3915150	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038	MYCT1, KATNA1, 422 more genes
nsv3920975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591	MYCT1, UST-AS2, 394 more genes
nsv3908622	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 150,284,435-170,919,470 , GRCh38.p12 chr6: 149,963,299-170,610,382	MYCT1, LOC105378120, 319 more genes
nsv3911164	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 135,720,981-155,817,943 , GRCh37 chr6: 135,679,288-155,776,251 , GRCh38 chr6: 135,358,150-155,455,117	MYCT1, HYMAI, 263 more genes
nsv3904213	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 151,214,792-170,892,243 , GRCh38.p12 chr6: 150,893,656-170,583,155	MYCT1, CTAGE13P, 304 more genes
nsv3913037	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 152,697,473-170,921,089 , GRCh38 chr6: 152,376,338-170,612,001 , NCBI36 chr6: 152,739,166-170,763,014	MYCT1, KRT8P44, 283 more genes
nsv4456488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 148,195,086-160,127,254 , GRCh38.p12 chr6: 147,873,950-159,706,222	MYCT1, PDCL3P5, 176 more genes
nsv4436131	complex substitution	1	nstd102	human	Pathogenic	GRCh38.p12 chr6: 151,122,197-170,745,979 , GRCh37 chr6: 151,443,333-171,115,067	MYCT1, ACAT2, 303 more genes
nsv4729446	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 151,472,860-154,839,846 , GRCh38.p12 chr6: 151,151,725-154,518,712	MYCT1, ESR1, 45 more genes
nsv3895460	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 152,702,696-153,345,479 , GRCh38.p12 chr6: 152,381,561-153,024,344	MYCT1, C11orf98P2, 12 more genes

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

Send to:

Search results

Items: 1 to 20 of 23

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 23

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity